Haemoscope Corp.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062604 | RAPIDTEG TEG-ACT TEST | JBP | 2007-01-31 | View |
| 510(k) | K041502 | THROMBELASTOGRAPH (TEG) PLATELET MAPPING ASSAY | JOZ | 2004-09-01 | View |
| 510(k) | K002177 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG-5000 SERIES | JPA | 2000-09-14 | View |
| 510(k) | K993678 | THROMBELASTOGRAPH COAGULATION ANALYZER TEG - 5000 SERIES | JPA | 2000-05-05 | View |
| 510(k) | K954437 | THROMBELASTOGRAPH COAGULATION ANALYZER 3000S | GKP | 1996-01-30 | View |
| 510(k) | K904204 | THROMBELASTOGRAPH | GKP | 1990-11-01 | View |
| 510(k) | K895844 | THROMBELASTOGRAPH(R) | GKP | 1989-10-24 | View |
No matching devices.
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