FDA 510(k)

BD PosiFlush Heparin Lock Flush Syringe

K-Number: K163591 · 2017-02-27

Decision Date2017-02-27

Product CodeNZW

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BD PosiFlush Heparin Lock Flush Syringe is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson and Company. It received FDA 510(k) clearance on 2017-02-27 under 510(k) number K163591. The device is classified under product code NZW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD PosiFlush Heparin Lock Flush Syringe?

BD PosiFlush Heparin Lock Flush Syringe is a medical device that received FDA 510(k) clearance on 2017-02-27. The listed applicant is Becton, Dickinson and Company. The 510(k) number is K163591.

When did BD PosiFlush Heparin Lock Flush Syringe receive FDA 510(k) clearance?

BD PosiFlush Heparin Lock Flush Syringe received FDA 510(k) clearance on 2017-02-27, under 510(k) number K163591.

Who is the listed applicant for BD PosiFlush Heparin Lock Flush Syringe?

The FDA 510(k) record lists Becton, Dickinson and Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD PosiFlush Heparin Lock Flush Syringe?

The FDA product code for BD PosiFlush Heparin Lock Flush Syringe is NZW.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.