GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE
K-Number: K991843 · 1999-06-25
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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