The Code of Federal Regulations of the United States of AmericaThe Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
No grāmatas satura
1.5. rezultāts no 5.
169. lappuse
136 that has been determined to contain no deficiencies that prevent the
Commissioner from making a decision on it . ... on animals and humans and from
all studies and tests of the device itself intended to establish or determine its
safety and ...
136 that has been determined to contain no deficiencies that prevent the
Commissioner from making a decision on it . ... on animals and humans and from
all studies and tests of the device itself intended to establish or determine its
safety and ...
235. lappuse
A hemoglobin A2 assay is a device used to determine the hemoglobin A , content
of human blood . ... reagents , apparatus , instrumentation , and controls
necessary to isolate and identify abnormal genetically determined hemoglobin
types .
A hemoglobin A2 assay is a device used to determine the hemoglobin A , content
of human blood . ... reagents , apparatus , instrumentation , and controls
necessary to isolate and identify abnormal genetically determined hemoglobin
types .
247. lappuse
... or ceptibility system . are used to determine immunity , or the assay is intended
for use in matrices ( a ) Identification . ... of of antimicrobial agents into a system
for the purpose of determining in vitro care ) . susceptibility of bacterial pathogens
...
... or ceptibility system . are used to determine immunity , or the assay is intended
for use in matrices ( a ) Identification . ... of of antimicrobial agents into a system
for the purpose of determining in vitro care ) . susceptibility of bacterial pathogens
...
536. lappuse
A device so labeled , however , that is determined by the Food and Drug
Administration to be intended for human use , will be considered to be a banned
device . In determining whether such a device is intended for human use , the
Food and ...
A device so labeled , however , that is determined by the Food and Drug
Administration to be intended for human use , will be considered to be a banned
device . In determining whether such a device is intended for human use , the
Food and ...
570. lappuse
This additional mammography review will help the agency to determine whether
the facility is in compliance with this ... ( 2 ) If FDA determines that the quality of
mammography performed by a facility , whether or not certified under $ 900 .
This additional mammography review will help the agency to determine whether
the facility is in compliance with this ... ( 2 ) If FDA determines that the quality of
mammography performed by a facility , whether or not certified under $ 900 .
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Populāri fragmenti
11. lappuse - Insufficiency of label space for the prominent placing of such word, statement, or information, resulting from the use of label space for any word, statement, design, or device which is not required by or under authority of the act to appear on the label; (5) Insufficiency of label space for the...
18. lappuse - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
356. lappuse - Act. (b) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21, unless otherwise noted.
86. lappuse - In computing any period of time prescribed or allowed by this part, the day of the act, event, or default after which the designated period of time begins to run is not to be included. The last day of the period so computed is to be included, unless it is...
79. lappuse - label" means a display of written, printed, or graphic matter upon the immediate container of any substance; and a requirement made by or under authority of this Act that any word, statement, or other information appear on the label shall not be considered to be complied with unless such word, statement, or other information also appears...
578. lappuse - Nothing in this section shall authorize the withholding of information by the Secretary or any officer or employee under his control, from the duly authorized committees of the Congress.
15. lappuse - On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound; in the case of fluid measure, it shall be expressed in the largest whole unit...
15. lappuse - 6 oz net wt.," and "6 fl oz" or "net contents 6 fl oz". (j) On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound...
56. lappuse - (1) the term 'manufacture, preparation, propagation, compounding, or processing' shall include repackaging or otherwise changing the container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person who makes final delivery or sale to the ultimate consumer; "(2) the term 'name...
Bibliogrāfiskā informācija
| Nosaukums | The Code of Federal Regulations of the United States of America |
| Atbalstītāji | United States. Division of the Federal Register, United States. Federal Register Division, United States. Office of the Federal Register |
| Izdevējs | U.S. Government Printing Office, 2006 |
| ISBN | 0160758246, 9780160758249 |
| Eksportēt avotu | BiBTeX EndNote RefMan |