TORAY ANTHRON ANGIOGRAPHIC CATHETERS

Cannula, Catheter

TORAY INDUSTRIES (AMERICA), INC.

The following data is part of a premarket notification filed by Toray Industries (america), Inc. with the FDA for Toray Anthron Angiographic Catheters.

Pre-market Notification Details

Device IDK872983
510k NumberK872983
Device Name:TORAY ANTHRON ANGIOGRAPHIC CATHETERS
ClassificationCannula, Catheter
Applicant TORAY INDUSTRIES (AMERICA), INC. 280 PARK AVE. New York,  NY  10017
ContactKohki Ueno
CorrespondentKohki Ueno
TORAY INDUSTRIES (AMERICA), INC. 280 PARK AVE. New York,  NY  10017
Product CodeDQR  
CFR Regulation Number870.1300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1987-07-31
Decision Date1987-11-20

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