BYO
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Bottle, Blow
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5220
- Medical specialty
- Anesthesiology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| EPIDURAL MINIPACK (K924541) | Concord/Portex | 1993-07-09 |
| HYPERFREE (K913527) | Kist Intl. | 1992-01-21 |
| BOTTLE BREATHING DEVICE (K780558) | B & F Medical Products, Inc. | 1978-05-26 |
| 2C7125 BLOW BOTTLE (K780407) | Travenol Laboratories, S.A. | 1978-04-10 |
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Every clearance here is in the API, with alerts when new ones post.