VISTA BRITE TIP CATHETERS

Catheter, Percutaneous

CORDIS CORP.

The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Vista Brite Tip Catheters.

Pre-market Notification Details

Device IDK965211
510k NumberK965211
Device Name:VISTA BRITE TIP CATHETERS
ClassificationCatheter, Percutaneous
Applicant CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes,  FL  33014
ContactKatherine Trevisol
CorrespondentKatherine Trevisol
CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes,  FL  33014
Product CodeDQY  
CFR Regulation Number870.1250 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-12-27
Decision Date1997-03-11
Summary:summary

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