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Catheters, Salpingography

FDA product code MOV · Class 2 · Obstetrics/Gynecology

4
Registered devices
19
Adverse events
3
Recalls
5
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-04-15Cook Inc.Increase in reports of polymer degradation of the catheter tip, resulting in tip fracture and/or separation. degradation could include loss of device function,
2010-01-08Cook Women'S HealthThe distal tip may separate from the catheter while the catheter is in the patient.
2010-01-08Cook Women'S HealthThe distal tip may separate from the catheter while the catheter is in the patient.

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