Code of Federal Regulations 21 Parts 800 to 1299 Food and Drugs: Revised as of April 1 2006U.S. Government Printing Office, 2006 - 796 lappuses The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the United States Federal Government. This volumwe contains the regulations about medical devices. |
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639. lappuse
... designed for one image re- ceptor size . Radiographic equipment designed for only one image receptor size at a fixed SID shall be provided with means to limit the field at the plane of the image receptor to dimensions no greater than ...
... designed for one image re- ceptor size . Radiographic equipment designed for only one image receptor size at a fixed SID shall be provided with means to limit the field at the plane of the image receptor to dimensions no greater than ...
640. lappuse
... designed . Each such device shall have clear and permanent markings to indicate the image receptor size and SID for which it is designed ; or ( iii ) A beam - limiting device having mul- tiple fixed apertures sufficient to meet the ...
... designed . Each such device shall have clear and permanent markings to indicate the image receptor size and SID for which it is designed ; or ( iii ) A beam - limiting device having mul- tiple fixed apertures sufficient to meet the ...
654. lappuse
... designed primarily for the in- spection of carry - on baggage are appli- cable to such systems manufactured or assembled on or after April 25 , 1974 . The provisions of this section are not applicable to systems which are de- signed ...
... designed primarily for the in- spection of carry - on baggage are appli- cable to such systems manufactured or assembled on or after April 25 , 1974 . The provisions of this section are not applicable to systems which are de- signed ...
Saturs
1 For nomenclature changes to chapter I see 59 FR 14366 Mar 28 1994 | 3 |
Labeling | 13 |
Medical device reporting | 38 |
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AC-powered accessories accreditation body amended at 65 ance standards application blood cardiopulmonary bypass catheter chapter subject Class II perform Class II special Classification clinical clude commercial distribution complaint files component current good manufacturing Date PMA dental denture device intended device is exempt device that consists disease electronic equipment facility FDA's fluoroscopic Food and Drug guidance document Identification image receptor immunological test system implanted intended for medical intended to measure July 25 labeling limitations mammography manufacturing practice manufacturing practice regula means medical purposes ment monitor notice of completion paragraph patient PDP is required plasma PMA or notice postmarket surveillance premarket approval premarket notification procedures procedures in subpart prosthesis radiation reagents regulation requirements concerning records respect to complaint Sept serological serum special controls specific submit subpart E surgical tion tissue trols type of device vice x-ray system