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FDA 510(k)

GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE

K-Number: K991843 · 1999-06-25

Decision Date1999-06-25
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE 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 1999-06-25 under 510(k) number K991843. 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 GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE?

GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE is a medical device that received FDA 510(k) clearance on 1999-06-25. The listed applicant is Greiner Meditech, Inc.. The 510(k) number is K991843.

When did GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE receive FDA 510(k) clearance?

GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE received FDA 510(k) clearance on 1999-06-25, under 510(k) number K991843.

Who is the listed applicant for GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE?

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 GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE?

The FDA product code for GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE is JKA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Greiner Meditech, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 10 devices →

Related Devices (Code: JKA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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