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Microfilter, Blood Transfusion

FDA product code CAK · Class 2 · General Hospital

49
Registered devices
1,648
Adverse events
1
Recalls
36
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-11-03GVS TM, IncDue to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.

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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.