FDA Device Intelligence
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Device, Urine Flow Rate Measuring, Non-Electrical, Disposable

FDA product code FFG · Class 2 · Gastroenterology, Urology

32
Registered devices
557
Adverse events
1
Recalls
17
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-12-04Cardinal Health 200, LLCConvenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

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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.