1 device · 1 company · 1995
Product code NMN: Instrument, Clip, Forming/Cutting, Reprocessed
1 device under product code NMN, 1995, from 1 company. Each record carries FDA's decision, the Indications for Use statement verbatim where the public document carries one (0 of 1 here), the regulation, and MAUDE report counts by product code.
Instrument, Clip, Forming/Cutting, Reprocessed. 21 CFR 882.4190, Class I. 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). MAUDE held 0 adverse-event reports against this product code as of 2026-10-29; reports are unverified and the code is shared by every device of this type.
Retrieved from FDA public records.
Every device, newest decision first
| Decision | Device | Company | Panel | FDA |
|---|---|---|---|---|
| AUTOPAPP950009 · PMA | BD DIAGNOSTICS | Pathology | database entry |
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