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FDA 510(k) Applications Submitted by JACQUELINE ZIMOVAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K971572
04/30/1997
VISTA BRITE TIP CATHETERS
CORDIS CORP.
K032340
07/29/2003
VISTAKON (GALYFILCON A) SOFT CONTACT LENS
JOHNSON & JOHNSON VISION CARE, INC.
K973401
09/09/1997
TEMPO 4 ANGIOGRAPHY CATHETER (VARIOUS)
CORDIS CORP.
K973845
10/08/1997
CORDIS HYDRONOL STEERABLE GUIDEWIRE
CORDIS CORP.
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