FDA 510(k)

VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES

K-Number: K061483 · 2006-08-14

ApplicantGreiner Bio-One North America, Inc.

Decision Date2006-08-14

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES 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 2006-08-14 under 510(k) number K061483. 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 VISIO PLUS BLOOD COLLECTION NEEDLES?

VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES is a medical device that received FDA 510(k) clearance on 2006-08-14. The listed applicant is Greiner Bio-One North America, Inc.. The 510(k) number is K061483.

When did VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES receive FDA 510(k) clearance?

VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES received FDA 510(k) clearance on 2006-08-14, under 510(k) number K061483.

Who is the listed applicant for VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES?

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 VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES?

The FDA product code for VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES 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.