PEQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Accessories To Examination Light
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6320
- Medical specialty
- General Hospital
- FDA definition
- Accessories that attach to the light and assist in magnifying, clarifying, enhancing the image being viewed.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| DERMA HOOD (K131338) | Globalmedia Group, LLC | 2013-07-10 | + Add |
Track PEQ automatically
Every clearance here is in the API, with alerts when new ones post.