FDA 510(k)

MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

K-Number: K022875 · 2002-09-11

Decision Date2002-09-11

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION 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 2002-09-11 under 510(k) number K022875. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET?

MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 2002-09-11. The listed applicant is Becton, Dickinson & CO. The 510(k) number is K022875.

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

MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET received FDA 510(k) clearance on 2002-09-11, under 510(k) number K022875.

Who is the listed applicant for MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION 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 MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET?

The FDA product code for MODIFICATION TO BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET is JKA.

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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.