FDA 510(k)

VAKU-8 BLOOD COLLECTION NEEDLES

K-Number: K090426 · 2009-06-12

Decision Date2009-06-12

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

VAKU-8 BLOOD COLLECTION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 2009-06-12 under 510(k) number K090426. 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 VAKU-8 BLOOD COLLECTION NEEDLES?

VAKU-8 BLOOD COLLECTION NEEDLES is a medical device that received FDA 510(k) clearance on 2009-06-12. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K090426.

When did VAKU-8 BLOOD COLLECTION NEEDLES receive FDA 510(k) clearance?

VAKU-8 BLOOD COLLECTION NEEDLES received FDA 510(k) clearance on 2009-06-12, under 510(k) number K090426.

Who is the listed applicant for VAKU-8 BLOOD COLLECTION NEEDLES?

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

What is the FDA product code for VAKU-8 BLOOD COLLECTION NEEDLES?

The FDA product code for VAKU-8 BLOOD COLLECTION NEEDLES is FMI.

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Related Devices (Code: FMI)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.