Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 1982 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
Citi izdevumi - Skatīt visu
Bieži izmantoti vārdi un frāzes
52 Stat 90 Stat accessible emission limits amended ance standards applicable ASTM ation blood Bureau Cardiopulmonary bypass catheter cation cell centimeters chapter Class II perform Class III premar Classification clude collateral radiation Commissioner compliance comply components containers controls Department designed determine device intended diagnostic distributor Drug Administration effective electronic product emission duration equipment exposure FEDERAL REGISTER fetal fluoroscopic Food and Drug Health hearing aid human access Identification image receptor intraocular lens investigational study ket approval labeling laser product laser radiation lens limits of Class manufac manufacturer manufacturing practice means measure medical device ment monitor nanometers Office operation pacemaker panel paragraph patient person platelet premarket notification procedures quirements radiant power radiation in excess records regulation requirements safety samples Secs Sept Service specific sponsor statement submitted tion tube type of device ultrasonic wavelength x-ray system x-ray tube
Populāri fragmenti
285. lappuse - That all charges for storage, cartage and labor on goods which are refused admission or delivery shall be paid by the owner or consignee, and in default of such payment shall constitute a...
212. lappuse - Secretary or any officer or employee under his control, from the duly authorized committees of the Congress.
112. lappuse - III (premarket approval), depending upon the level of regulatory control required to provide reasonable assurance of the safety and effectiveness of the device (§860.3(c)). This subpart does not apply to a device that is classified into class III by statute under section 513(f) of the act because the Food and Drug Administration has determined that the device is not "substantially equivalent...
271. lappuse - Cream is that portion of milk, rich in milk fat, which rises to the surface of milk on standing, or is separated from it by centrifugal force, is fresh and clean and contains not less than eighteen (18) per cent of milk fat.
224. lappuse - Hearing. (a) If it appears that the article may be subject to refusal of admission, the district director shall give the owner or consignee a written notice to that effect, stating the reasons therefor. The notice shall specify a place and a period of time during which the owner or consignee shall have an opportunity to introduce testimony. Upon timely request, giving reasonable grounds therefor, such time and place may be changed. Such testimony shall be confined to matters relevant to the admissibility...
281. lappuse - Secretary of the Treasury, and if such board shall, after due examination, find the tea in question to be equal in purity, quality, and fitness for consumption to the...
271. lappuse - Milk is the fresh, clean, lacteal secretion obtained by the complete milking of one or more healthy cows, properly fed and kept, excluding that obtained within fifteen days before and...
14. lappuse - ... (quarts, quarts and pints. or pints, as appropriate) with any remainder in terms of fluid ounces or common or decimal fractions of the pint or quart (see examples in paragraphs (m) (3) and (4) of this section).
16. lappuse - If a shipment or delivery, or any part thereof, of a drug or device which is exempt under the regulations in this section is made to a person in whose possession the article is not exempt, or is made for any purpose other than those specified, such exemption shall expire, with respect to such shipment or delivery or part thereof, at the beginning of that shipment or delivery.
45. lappuse - Except as provided in subsection (b), no State or political subdivision of a State may establish or continue in effect with respect to a device intended for human use any requirement— (1) which is different from, or in addition to, any requirement applicable under this...