| [Code of Federal Regulations] |
| [Title 21, Volume 8] |
| [Revised as of April 1, 2012] |
| [CITE: 21CFR801.119] |
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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. 801.119 In vitro diagnostic products.
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A product intended for use in the diagnosis of disease and which is an in vitro diagnostic product as defined in 809.3(a) of this chapter shall be deemed to be in compliance with the requirements of this section and section 502(f)(1) of the act if it meets the requirements of 809.10 of this chapter.
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