| [Code of Federal Regulations] |
| [Title 21, Volume 8] |
| [Revised as of April 1, 2012] |
| [CITE: 21CFR820.5] |
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CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES |
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| SUBCHAPTER H--MEDICAL DEVICES |
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PART 820 -- QUALITY SYSTEM REGULATION
Subpart A--General Provisions
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Sec. 820.5 Quality system.
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Each manufacturer shall establish and maintain a quality system that is appropriate for the specific medical device(s) designed or manufactured, and that meets the requirements of this part.
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