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Transducer, Ultrasonic

FDA product code JOP · Class 2 · Cardiovascular

435
Registered devices
24
Adverse events
1
Recalls
72
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-06-26Biosound Esaote, Inc.Using the PA230E transducer with a user-defined setting with the output power to 100% (Max) in 2D-TEI mode focusing at maximum depth, could cause the transducer

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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.