IDM
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Microtome, Ultra
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.3010
- Medical specialty
- Pathology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| LKB-BROMMA 2188 ULTROTOME NOVA (K812158) | Lkb Instruments, Inc. | 1981-09-16 |
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Every clearance here is in the API, with alerts when new ones post.