GBJ
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Prosthesis, Adhesive, External
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.3750
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DUET (K934970) | Trulife , Ltd. | 1993-12-10 |
| OPERATING TABLE ACCESSORY CLAMP (K810282) | Minnesota Scientific, Inc. | 1981-02-26 |
| GORDON IVS INTRAVENOUS STABILIZER (K790946) | Whitman Medical Corp. | 1979-06-05 |
| PROTECTIVSTABILIZER (K790186) | Jelco Laboratories | 1979-02-26 |
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Every clearance here is in the API, with alerts when new ones post.