FDA product code DRP: Tourniquet, Automatic Rotating
DRP is the FDA product code for tourniquet, automatic rotating. It is a Class II device, regulated under 21 CFR 870.5925 and reviewed by the Cardiovascular panel. Devices under DRP reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Tourniquet, Automatic Rotating |
| Device class | Class II |
| Regulation | 21 CFR 870.5925 |
| Review panel | CV — Cardiovascular |
| Medical specialty | Cardiovascular |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for DRP devices
openFDA lists no recalls for product code DRP.
Frequently asked questions
What is FDA product code DRP?
DRP is the FDA product code for tourniquet, automatic rotating. It is a Class II device, regulated under 21 CFR 870.5925 and reviewed by the Cardiovascular panel.
What device class is DRP?
Class II, regulation 21 CFR 870.5925. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code DRP
- Run a recall and safety report across every DRP manufacturer
- Watch product code DRP 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.
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