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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