GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE— 510(k) K991843

Substantially Equivalent

Greiner Meditech, Inc.

FDA 510(k) clearance K991843 for GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE, Substantially Equivalent on 1999-06-25. Applicant: Greiner Meditech, Inc..

Clearance details

Applicant: Greiner Meditech, Inc.
Product code: Code JKA
Advisory panel: Clinical Chemistry
Date received: 1999-05-28
Decision date: 1999-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bel Air, MD, US

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Adverse events under product code JKA

product code JKA

Injury: 455
Malfunction: 26,686
Other: 4
Total: 27,145

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.