HCE
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Clamp, Carotid Artery
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 882.5175
- Medical specialty
- Neurology
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SELVERSTONE CLAMP SALIBI CLAMP (K870399) | Codman & Shurtleff, Inc. | 1987-03-06 |
| CAROTID ARTERY CLAMP & TOOLS (K811821) | New England Surgical Instrument Corp. | 1981-09-24 |
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Every clearance here is in the API, with alerts when new ones post.