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Bentec Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002650VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726February 16, 2001
K971411DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS CATHETER KIT V-27030KJune 3, 1997
K971517SILICONE PUTTY EAR PLUGSJune 2, 1997