| [Code of Federal Regulations] |
| [Title 21, Volume 8] |
| [Revised as of April 1, 2012] |
| [CITE: 21CFR801.122] |
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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 801 -- LABELING
Subpart D--Exemptions From Adequate Directions for Use
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Sec. 801.122 Medical devices for processing, repacking, or manufacturing.
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A device intended for processing, repacking, or use in the manufacture of another drug or device shall be exempt from section 502(f)(1) of the act if its label bears the statement "Caution: For manufacturing, processing, or repacking".
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