FDA 510(k)

GREINER VACUETTE QUICKSHIELD COMPLETE

K-Number: K072320 · 2007-09-14

ApplicantGreiner Bio-One North America, Inc.

Decision Date2007-09-14

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

GREINER VACUETTE QUICKSHIELD COMPLETE is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Bio-One North America, Inc.. It received FDA 510(k) clearance on 2007-09-14 under 510(k) number K072320. 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 GREINER VACUETTE QUICKSHIELD COMPLETE?

GREINER VACUETTE QUICKSHIELD COMPLETE is a medical device that received FDA 510(k) clearance on 2007-09-14. The listed applicant is Greiner Bio-One North America, Inc.. The 510(k) number is K072320.

When did GREINER VACUETTE QUICKSHIELD COMPLETE receive FDA 510(k) clearance?

GREINER VACUETTE QUICKSHIELD COMPLETE received FDA 510(k) clearance on 2007-09-14, under 510(k) number K072320.

Who is the listed applicant for GREINER VACUETTE QUICKSHIELD COMPLETE?

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

What is the FDA product code for GREINER VACUETTE QUICKSHIELD COMPLETE?

The FDA product code for GREINER VACUETTE QUICKSHIELD COMPLETE is FMI.

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Other records listing Greiner Bio-One North America, Inc. as applicant

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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.