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FDA 510(k) Applications Submitted by KATHERINE TREVISOL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K962362
06/19/1996
CORDIS ENVOY & VISTA BRITE TIP GUIDING CATHETERS
CORDIS CORP.
K962830
07/22/1996
VISTA BRITE TIP CATHETERS
CORDIS CORP.
K972978
08/11/1997
VISTA BRITE TIP GUIDING CATHETERS
CORDIS CORP.
K963962
10/02/1996
VISTA BRITE TIP CATHETERS
CORDIS CORP.
K965211
12/27/1996
VISTA BRITE TIP CATHETERS
CORDIS CORP.
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