FDA 510(k)

PACT SUPPLEMENT

K-Number: K810591 · 1981-03-20

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1981-03-20

Product CodeJSK

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

PACT SUPPLEMENT 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 1981-03-20 under 510(k) number K810591. The device is classified under product code JSK. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACT SUPPLEMENT?

PACT SUPPLEMENT is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K810591.

When did PACT SUPPLEMENT receive FDA 510(k) clearance?

PACT SUPPLEMENT received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810591.

Who is the listed applicant for PACT SUPPLEMENT?

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 PACT SUPPLEMENT?

The FDA product code for PACT SUPPLEMENT is JSK.

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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.