FDA 510(k)

BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET

K-Number: K011984 · 2001-08-29

Decision Date2001-08-29

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Becton, Dickinson & CO. It received FDA 510(k) clearance on 2001-08-29 under 510(k) number K011984. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET?

BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET is a medical device that received FDA 510(k) clearance on 2001-08-29. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K011984.

When did BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET receive FDA 510(k) clearance?

BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET received FDA 510(k) clearance on 2001-08-29, under 510(k) number K011984.

Who is the listed applicant for BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET?

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

What is the FDA product code for BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET?

The FDA product code for BD VACUTAINER PUSH BUTTON BLOOD COLECTION SET is FMI.

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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.