MZT
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Heimlich Maneuver Assist
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5115
- Medical specialty
- Anesthesiology
- Flags
- Life-sustaining
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| Record | Firm | Date | Builder |
|---|---|---|---|
| QUICKAIR CHOKE RELIEVER, MODEL 59-001A (DEN000004) | Maet Industries, Inc. | 2000-02-29 |
Track MZT automatically
Every clearance here is in the API, with alerts when new ones post.