FDA product code NMM: Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed
NMM is the FDA product code for catheter, angioplasty, peripheral, transluminal, reprocessed. It is a Class II device, regulated under 21 CFR 870.1250 and reviewed by the Cardiovascular panel. Devices under NMM reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf)
Classification
| Field | Value |
|---|---|
| Device name | Catheter, Angioplasty, Peripheral, Transluminal, Reprocessed |
| Device class | Class II |
| Regulation | 21 CFR 870.1250 |
| Review panel | CV — Cardiovascular |
| Medical specialty | Cardiovascular |
| Premarket route | 510(k) |
Recalls for NMM devices
openFDA lists no recalls for product code NMM.
Frequently asked questions
What is FDA product code NMM?
NMM is the FDA product code for catheter, angioplasty, peripheral, transluminal, reprocessed. It is a Class II device, regulated under 21 CFR 870.1250 and reviewed by the Cardiovascular panel.
What device class is NMM?
Class II, regulation 21 CFR 870.1250. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NMM
- Run a recall and safety report across every NMM manufacturer
- Watch product code NMM 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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