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Guidewire, Catheter, Reprocessed

FDA product code NKQ · Class 2 · Cardiovascular

1
Registered devices
4
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

RIVA Posterior Fixation System — XENIX MEDICAL LLC

Recent recalls

DateFirmReason
2021-05-04Medtronic VascularThe component part numbers intended for shipment to a third-party, where they are further processed into kits and sterilized were instead shipped directly to cu

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.