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Imager, Ultrasonic Obstetric-Gynecologic

FDA product code HEM · Class 2 · Obstetrics/Gynecology

3
Registered devices
1
Adverse events
1
Recalls
30
510(k) clearances

Devices with this code

Transducer Cover — Vitrolife Sweden ABTransducer Cover — Vitrolife Sweden ABTransducer Cover — Vitrolife Sweden AB

Recent recalls

DateFirmReason
2008-05-12Digisonics, IncData/measurements from a OB report sent from ultrasound systems populated the wrong OB-View report

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.