FTZ
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Locator, Magnetic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.4445
- Medical specialty
- Ophthalmic
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SUN BED BY VERRE ET QUARTZ UVA-FRANCE (K833229) | H & M Douglas Enterprises, Inc. | 1984-01-27 |
| MODEL 200 (K830468) | Western Laboratories Corp. | 1983-04-12 |
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Every clearance here is in the API, with alerts when new ones post.