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FDA 510(k) Applications Submitted by DAVID TUCKER
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.
K991291
04/15/1999
STRETTA INFLATABLE BASKET CATHETER ELECTRODE WITH ASPIRATION
CONWAY STUART MEDICAL, INC.
K991529
05/03/1999
CSM STRETTA CONTROL MODULE ELECTROSURGICAL GENERATOR, MODEL S400
CONWAY STUART MEDICAL, INC.
K983871
11/02/1998
RITA MODEL 70 ELECTROSURGICAL PROBE
RITA MEDICAL SYSTEMS
K955121
11/09/1995
HEARTPORT ENDOARTERIAL RETURN CANNUAL
HEARTPORT, INC.
K955132
11/09/1995
HEARTPORT ENDOAORTIC CLAMP
HEARTPORT, INC.
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