JZB
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scissors, Ear
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACK (K914226) | E.I. Dupont DE Nemours & Co., Inc. | 1991-11-19 |
| VEIN GRAFT EAR SCISSORS (K870756) | Treace Medical, Inc. | 1987-03-03 |
| SCISSORS SHEA BELLUCC (K833603) | Microtek Medical, Inc. | 1984-01-03 |
| EAR SCISSORS (K822196) | Kelleher Corp. | 1982-08-30 |
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Every clearance here is in the API, with alerts when new ones post.