FDA 510(k)

VACUTAINER PLUS WITH HEMOGARD CLOSURE

K-Number: K901449 · 1990-08-09

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1990-08-09

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

VACUTAINER PLUS WITH HEMOGARD CLOSURE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1990-08-09 under 510(k) number K901449. 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 VACUTAINER PLUS WITH HEMOGARD CLOSURE?

VACUTAINER PLUS WITH HEMOGARD CLOSURE is a medical device that received FDA 510(k) clearance on 1990-08-09. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K901449.

When did VACUTAINER PLUS WITH HEMOGARD CLOSURE receive FDA 510(k) clearance?

VACUTAINER PLUS WITH HEMOGARD CLOSURE received FDA 510(k) clearance on 1990-08-09, under 510(k) number K901449.

Who is the listed applicant for VACUTAINER PLUS WITH HEMOGARD CLOSURE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUTAINER PLUS WITH HEMOGARD CLOSURE?

The FDA product code for VACUTAINER PLUS WITH HEMOGARD CLOSURE is JKA.

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Official Source

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