EAQ
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Detector, Ultraviolet
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.6350
- Medical specialty
- Dental
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SUNSOR ULTRAVIOLET METER (K934728) | Sunsor, Inc. | 1994-07-28 |
| LIGHT, EXAMINING, DENTAL, ULTRA VIOLET (K770685) | Parker Laboratories, Inc. | 1977-04-26 |
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Every clearance here is in the API, with alerts when new ones post.