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Cystometer, Electrical Recording

FDA product code EXQ · Class 2 · Gastroenterology, Urology

37
Registered devices
9
Adverse events
1
Recalls
8
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2009-04-09Laborie Medical Technologies CorLaborie Medical Technologies reports that there was a mix up in the labeling and packaging of their Urodynamic Catheters. There were 8Fr catheters mixed inside

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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.