HQQ
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Apparatus, Cautery, Radiofrequency, Battery-Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.4100
- Medical specialty
- Ophthalmic
- Flags
- Third-party review eligible
- Adverse events (MAUDE)
- 1992: 1 · 1993: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SCITECH BI-MANUAL ADAPTER CLIPS (K910088) | Scitech Industries Partnership | 1991-04-08 |
| MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTAT (K903878) | Mentor O & O, Inc. | 1990-11-05 |
| MENTOR WET-FIELD*II COAGULATOR (K881001) | Mentor O & O, Inc. | 1988-05-13 |
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Every clearance here is in the API, with alerts when new ones post.