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FDA 510(k) Applications Submitted by BENTEC MEDICAL, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002650
08/25/2000
VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726
BENTEC MEDICAL, INC.
K971411
04/16/1997
DISPOSABLE SILICONE EPISTAXIS CATHETER V-27030/DISPOSABLE SILICONE EPISTAXIS CATHETER KIT V-27030K
BENTEC MEDICAL, INC.
K971517
04/25/1997
SILICONE PUTTY EAR PLUGS
BENTEC MEDICAL, INC.
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