FDA product code NMI: Laparoscopic Insufflator And Accessories, Reprocessed
NMI is the FDA product code for laparoscopic insufflator and accessories, reprocessed. It is a Class I device, regulated under 21 CFR 884.1730 and reviewed by the Obstetrics and Gynecology panel. Devices under NMI reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Laparoscopic Insufflator And Accessories, Reprocessed |
| Device class | Class I |
| Regulation | 21 CFR 884.1730 |
| Review panel | OB — Obstetrics and Gynecology |
| Medical specialty | Obstetrics/Gynecology |
| Premarket route | 510(k) |
| Third-party 510(k) review eligible | Yes |
Recalls for NMI devices
openFDA lists no recalls for product code NMI.
Frequently asked questions
What is FDA product code NMI?
NMI is the FDA product code for laparoscopic insufflator and accessories, reprocessed. It is a Class I device, regulated under 21 CFR 884.1730 and reviewed by the Obstetrics and Gynecology panel.
What device class is NMI?
Class I, regulation 21 CFR 884.1730. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code NMI
- Run a recall and safety report across every NMI manufacturer
- Watch product code NMI 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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