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Acid, Uric, Acid Reduction Of Ferric Ion

FDA product code LFQ · Class 1 · Clinical Chemistry

12
Registered devices
1
Adverse events
1
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-07-20Sterling Diagnostics, Inc.Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple diagnostic kits due to a recision of the previously extended expiration dates for the k

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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.