BD SINGLE USE, HYPODERMIC SYRINGE

Syringe, Piston

Becton, Dickinson And Company

The following data is part of a premarket notification filed by Becton, Dickinson And Company with the FDA for Bd Single Use, Hypodermic Syringe.

Pre-market Notification Details

Device IDK110771
510k NumberK110771
Device Name:BD SINGLE USE, HYPODERMIC SYRINGE
ClassificationSyringe, Piston
Applicant Becton, Dickinson And Company 1 BECTON DRIVE MC237 Franklin Lakes,  NJ  07417
ContactJohn Roberts
CorrespondentJohn Roberts
Becton, Dickinson And Company 1 BECTON DRIVE MC237 Franklin Lakes,  NJ  07417
Product CodeFMF  
CFR Regulation Number880.5860 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2011-03-21
Decision Date2011-05-13
Summary:summary

NIH GUDID Devices

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