OSTOMY APPLIANCE BELT

Collector, Ostomy

E. R. SQUIBB & SONS, INC.

The following data is part of a premarket notification filed by E. R. Squibb & Sons, Inc. with the FDA for Ostomy Appliance Belt.

Pre-market Notification Details

Device IDK781088
510k NumberK781088
Device Name:OSTOMY APPLIANCE BELT
ClassificationCollector, Ostomy
Applicant E. R. SQUIBB & SONS, INC. 40 W 57TH ST. New York,  NY  10019
Product CodeEXB  
CFR Regulation Number876.5900 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1978-06-29
Decision Date1978-08-18

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