HMH
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Rack, Skiascopic
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 886.1750
- Medical specialty
- Ophthalmic
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SKIASCOPIC RACKS (K844364) | Luneau Laboratories | 1985-01-02 |
| VISITEC FLIERINGA-LEGRAND FIXATION RING (K843195) | Visitec Co. | 1984-10-05 |
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