FDA 510(k)

VACUETTE SAFETY BLOOD COLLECTION SET

K-Number: K011786 · 2001-07-12

ApplicantGreiner Vacuette North America, Inc.

Decision Date2001-07-12

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUETTE SAFETY BLOOD COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Vacuette North America, Inc.. It received FDA 510(k) clearance on 2001-07-12 under 510(k) number K011786. 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 SAFETY BLOOD COLLECTION SET?

VACUETTE SAFETY BLOOD COLLECTION SET is a medical device that received FDA 510(k) clearance on 2001-07-12. The listed applicant is Greiner Vacuette North America, Inc.. The 510(k) number is K011786.

When did VACUETTE SAFETY BLOOD COLLECTION SET receive FDA 510(k) clearance?

VACUETTE SAFETY BLOOD COLLECTION SET received FDA 510(k) clearance on 2001-07-12, under 510(k) number K011786.

Who is the listed applicant for VACUETTE SAFETY BLOOD COLLECTION SET?

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

What is the FDA product code for VACUETTE SAFETY BLOOD COLLECTION SET?

The FDA product code for VACUETTE SAFETY BLOOD COLLECTION SET 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.