KBC
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Saw, Nasal
- 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 |
|---|---|---|
| SKIN STAPLE EXTRACTOR (K811887) | Sierra Laboratories, Inc. | 1981-07-27 |
| AUTO SUTURE PSS SKIN STAPLING INSTRUMENT (K810187) | United States Surgical, A Division of Tyco Healthc | 1981-03-20 |
| AUTO SUTURE GAS POWERED DISP. LDS STAPL (K810188) | United States Surgical, A Division of Tyco Healthc | 1981-03-20 |
| JOSEPH SAW (K772379) | Edward Weck, Inc. | 1978-02-02 |
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Every clearance here is in the API, with alerts when new ones post.