FDA 510(k)

VACUETTE MULTIPLE SAMPLE LUER ADAPTER

K-Number: K981619 · 1998-07-15

Decision Date1998-07-15

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VACUETTE MULTIPLE SAMPLE LUER ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Greiner Meditech, Inc.. It received FDA 510(k) clearance on 1998-07-15 under 510(k) number K981619. 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 MULTIPLE SAMPLE LUER ADAPTER?

VACUETTE MULTIPLE SAMPLE LUER ADAPTER is a medical device that received FDA 510(k) clearance on 1998-07-15. The listed applicant is Greiner Meditech, Inc.. The 510(k) number is K981619.

When did VACUETTE MULTIPLE SAMPLE LUER ADAPTER receive FDA 510(k) clearance?

VACUETTE MULTIPLE SAMPLE LUER ADAPTER received FDA 510(k) clearance on 1998-07-15, under 510(k) number K981619.

Who is the listed applicant for VACUETTE MULTIPLE SAMPLE LUER ADAPTER?

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

What is the FDA product code for VACUETTE MULTIPLE SAMPLE LUER ADAPTER?

The FDA product code for VACUETTE MULTIPLE SAMPLE LUER ADAPTER 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.