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Monitor, Ultrasonic, Fetal

FDA product code KNG · Class 2 · Obstetrics/Gynecology

281
Registered devices
32
Adverse events
1
Recalls
60
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-10-06CooperSurgical, Inc.The 2MHZ prove was incorrectlhttp://cts.fda.gov/division-tracking/images/trash.pngy labeled as a 3MHZ probe

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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.