FDA product code MZT: Device, Heimlich Maneuver Assist
MZT is the FDA product code for device, heimlich maneuver assist. It is a Class II device, regulated under 21 CFR 868.5115 and reviewed by the Anesthesiology panel. Devices under MZT reach the market by 510(k) exempt; FDA lists no cleared 510(k)s for it. 1 De Novo request was granted under it.
Classification
| Field | Value |
|---|---|
| Device name | Device, Heimlich Maneuver Assist |
| Device class | Class II |
| Regulation | 21 CFR 868.5115 |
| Review panel | AN — Anesthesiology |
| Medical specialty | Anesthesiology |
| Premarket route | 510(k) exempt |
| Life-sustaining or supporting | Yes |
Recalls for MZT devices
openFDA lists no recalls for product code MZT.
Frequently asked questions
What is FDA product code MZT?
MZT is the FDA product code for device, heimlich maneuver assist. It is a Class II device, regulated under 21 CFR 868.5115 and reviewed by the Anesthesiology panel.
What device class is MZT?
Class II, regulation 21 CFR 868.5115. Typical premarket route: 510(k) exempt.
Next steps
- Run an FDA pathway report with predicate devices for product code MZT
- Run a recall and safety report across every MZT manufacturer
- Watch product code MZT for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
All Anesthesiology product codes · FDA product code lookup · 510(k) database search · 510(k) review times