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FDA 510(k) Applications Submitted by JODI L GREENIZEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020012
01/03/2002
MODIFICATION TO RENEGADE FIBER BRAIDED MICROCATHETER
BOSTON SCIENTIFIC/MEDI-TECH
K011664
05/30/2001
IMAGER II ANGIOGRAPHIC CATHETER
BOSTON SCIENTIFIC/MEDI-TECH
K003929
12/20/2000
NIROYAL BILIARY PREMOUNTED STENT SYSTEM
BOSTON SCIENTIFIC CORP.
K030083
01/09/2003
VAXCEL WITH PASV PORT
BOSTON SCIENTIFIC CORP.
K971010
03/20/1997
PERIPHERAL TRANSLUMINAL ANGIOPLASTY CATHETERS
CORDIS CORP.
K030966
03/27/2003
CONTOUR EMBOLI PVA AND FASTRACKER-325 INFUSION CATHETER
BOSTON SCIENTIFIC CORP.
K971579
04/21/1997
CORDIS OPTA 5 PTA BALLOON CATHETER
CORDIS CORP.
K031844
06/16/2003
VAXCEL WITH PASV PORT (LOW PROFILE), MODELS 45-236 AND 45-238
BOSTON SCIENTIFIC CORP.
K011906
06/19/2001
BACK-UP MEIER GUIDEWIRE
BOSTON SCIENTIFIC CORP.
K032008
06/30/2003
VAXCEL WITH PASV PORT, MODEL 45-213
BOSTON SCIENTIFIC CORP.
K022427
07/25/2002
CONTOUR SE MICROSPHERES
BOSTON SCIENTIFIC CORP.
K032375
08/01/2003
VAXCEL PORT, MODELS 45-336 AND 45-338
BOSTON SCIENTIFIC CORP.
K032542
08/18/2003
MODIFICATION TO CONTOUR SE MICROSPHERES
BOSTON SCIENTIFIC CORP.
K032600
08/25/2003
VAXCEL PORT, MODEL 45-333 AND VAXCEL W/PASV PORT, MODEL 45-233
BOSTON SCIENTIFIC CORP.
K032707
09/02/2003
CONTOUR SE MICROSPHERES (SYRINGE)
BOSTON SCIENTIFIC CORP.
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