GZQ
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Instrument, Dowel Cutting
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 882.4275
- Medical specialty
- Neurology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| FUJITENS III (K893874) | Altoona Medical Supply | 1989-12-22 |
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