Surgical devices · 21 CFR 872 Subpart E
Gas-Powered Jet Injector
FDA device type “Injector, Jet, Gas-Powered”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 10 in five years
- FDA name
- Injector, Jet, Gas-Powered
510(k) clearances per year, 1976–2026
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 9 Oct 1990 | K901348 | WILSON-COOK BRONCHOSCOPE BIOPSY FORCEPS | Wilson-Cook Medical, Inc. |
Official records: FDA product classification for EGQ · 21 CFR 872.4465.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026