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 ID: K110771
• 510k Number: K110771
• Device Name: BD SINGLE USE, HYPODERMIC SYRINGE
• Classification: Syringe, Piston
• Applicant: Becton, Dickinson And Company 1 BECTON DRIVE MC237 Franklin Lakes, NJ 07417
• Contact: John Roberts
• Correspondent: John Roberts; Becton, Dickinson And Company 1 BECTON DRIVE MC237 Franklin Lakes, NJ 07417
• Product Code: FMF
• CFR Regulation Number: 880.5860 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2011-03-21
• Decision Date: 2011-05-13
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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