FDA 510(k)

VACUETTE QUICKSHIELD SAFETY TUBE HOLDER

K-Number: K033478 · 2003-12-29

ApplicantGreiner Bio-One Vacuette North America

Decision Date2003-12-29

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUETTE QUICKSHIELD SAFETY TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Bio-One Vacuette North America. It received FDA 510(k) clearance on 2003-12-29 under 510(k) number K033478. 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 VACUETTE QUICKSHIELD SAFETY TUBE HOLDER?

VACUETTE QUICKSHIELD SAFETY TUBE HOLDER is a medical device that received FDA 510(k) clearance on 2003-12-29. The listed applicant is Greiner Bio-One Vacuette North America. The 510(k) number is K033478.

When did VACUETTE QUICKSHIELD SAFETY TUBE HOLDER receive FDA 510(k) clearance?

VACUETTE QUICKSHIELD SAFETY TUBE HOLDER received FDA 510(k) clearance on 2003-12-29, under 510(k) number K033478.

Who is the listed applicant for VACUETTE QUICKSHIELD SAFETY TUBE HOLDER?

The FDA 510(k) record lists Greiner Bio-One Vacuette North America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VACUETTE QUICKSHIELD SAFETY TUBE HOLDER?

The FDA product code for VACUETTE QUICKSHIELD SAFETY TUBE HOLDER 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.