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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28. lappuse
... hearing aids that use tubing , and in storing the hearing aid when it will not be used for an extended period of time . ( c ) Replacing or recharging the bat- teries , including a generic designation of replacement batteries . ( v ) ...
... hearing aids that use tubing , and in storing the hearing aid when it will not be used for an extended period of time . ( c ) Replacing or recharging the bat- teries , including a generic designation of replacement batteries . ( v ) ...
29. lappuse
... hearing aid dispenser , as appropriate , for a hearing aid evaluation . The audiologist or hearing aid dispenser will conduct a hearing aid evaluation to as- sess your ability to hear with and without a hearing aid . The hearing aid ...
... hearing aid dispenser , as appropriate , for a hearing aid evaluation . The audiologist or hearing aid dispenser will conduct a hearing aid evaluation to as- sess your ability to hear with and without a hearing aid . The hearing aid ...
30. lappuse
... Hearing aid devices ; condi- tions for sale . ( a ) Medical evaluation requirements— ( 1 ) General . Except as provided in para- graph ( a ) ( 2 ) of this section , a hearing aid dispenser shall not sell a hearing aid unless the ...
... Hearing aid devices ; condi- tions for sale . ( a ) Medical evaluation requirements— ( 1 ) General . Except as provided in para- graph ( a ) ( 2 ) of this section , a hearing aid dispenser shall not sell a hearing aid unless the ...
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