FDA 510(k)

MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES

K-Number: K063357 · 2007-07-10

ApplicantGreiner Bio-One North America, Inc.

Decision Date2007-07-10

Product CodeJKA

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES 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 2007-07-10 under 510(k) number K063357. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES?

MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES is a medical device that received FDA 510(k) clearance on 2007-07-10. The listed applicant is Greiner Bio-One North America, Inc.. The 510(k) number is K063357.

When did MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES receive FDA 510(k) clearance?

MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES received FDA 510(k) clearance on 2007-07-10, under 510(k) number K063357.

Who is the listed applicant for MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES?

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 MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES?

The FDA product code for MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES is JKA.

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

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Related Devices (Code: JKA)

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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.