GREINER MINICOLLECT LITHIUM HEPARIN GEL BLOOD COLLECTION TUBE— 510(k) K991843
Substantially EquivalentGreiner 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.. Device class: 2.
Clearance details
- Applicant
- Greiner Meditech, Inc.
- Product code
- Product code JKA
- Device class
- Class 2
- Regulation
- 21 CFR 862.1675
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bel Air, MD, US
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More clearances from Greiner Meditech, Inc.
view allAdverse events under product code JKA
product code JKA- Injury
- 455
- Malfunction
- 26,686
- Other
- 4
- Total
- 27,145
Source: openFDA MAUDE database, through . 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.