FDA 510(k)

BECTON DICKINSON TWINPAK

K-Number: K974006 · 1998-01-22

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic

Decision Date1998-01-22

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

BECTON DICKINSON TWINPAK 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 1998-01-22 under 510(k) number K974006. 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 BECTON DICKINSON TWINPAK?

BECTON DICKINSON TWINPAK is a medical device that received FDA 510(k) clearance on 1998-01-22. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K974006.

When did BECTON DICKINSON TWINPAK receive FDA 510(k) clearance?

BECTON DICKINSON TWINPAK received FDA 510(k) clearance on 1998-01-22, under 510(k) number K974006.

Who is the listed applicant for BECTON DICKINSON TWINPAK?

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 BECTON DICKINSON TWINPAK?

The FDA product code for BECTON DICKINSON TWINPAK is FMI.

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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.