Pacific Hemostasis
FDA 510(k) & PMA Approved Devices — 29 products
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Total Devices29
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K000679 | THROMBOSTRATE CONTROL PLASMAS | GGN | 2000-03-24 | View |
| 510(k) | K994100 | PACIFIC HEMOSTASIS THROMBOPLASTIN D | GJS | 2000-02-18 | View |
| 510(k) | K992130 | PACIFIC HEMOSTASIS THROMBOSCREEN 400C | KQG | 1999-09-03 | View |
| 510(k) | K992279 | HEPARIN CONTROL PLASMA LEVEL 2 | GGN | 1999-08-26 | View |
| 510(k) | K992278 | HEPARIN CONTROL PLASMA LEVEL 1 | GGN | 1999-08-26 | View |
| 510(k) | K991321 | PACIFIC HEMOSTASIS THROMBOSCREEN 200 | KQG | 1999-06-21 | View |
| 510(k) | K990046 | PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR VIII DEFICIENT PLASMA | GJT | 1999-02-17 | View |
| 510(k) | K984131 | COAGULATION CONTROL LEVEL 3 (ABNORMAL) | GGC | 1998-12-01 | View |
| 510(k) | K984129 | COAGULATION CONTROL LEVEL 1 (NORMAL) | GIZ | 1998-12-01 | View |
| 510(k) | K984130 | COAGULATION CONTROL LEVEL 2 (ABNORMAL) | GGC | 1998-12-01 | View |
| 510(k) | K972627 | PACIFIC HEMOSTASIS IMMUNODEPLETED FACTOR V DEFICIENT PLASMA (THROMBOSDREEN BRAND) (100056) | GJT | 1997-08-13 | View |
| 510(k) | K971428 | COAGULATION CONTROL PLASMA(ABNORMAL)LEVEL 0 | GGN | 1997-06-17 | View |
| 510(k) | K940082 | THROMBOSCREEN THROMBOPLASTIN-DS | GJS | 1995-02-14 | View |
| 510(k) | K891337 | THROMBOSCREEN APTT REAGENT | GFO | 1989-04-21 | View |
| 510(k) | K872217 | THROMBOSCREEN JOSHUA HEMOGLOBIN S SCREENING KIT | GHM | 1987-07-31 | View |
| 510(k) | K864643 | GLYCOSCREEN GLYCOSYLATED HEMOGLOBIN ASSAY KIT | LCP | 1987-04-28 | View |
| 510(k) | K854079 | THROMBO SCREEN SICKLE CELL ASSAY SET | GHM | 1985-10-31 | View |
| 510(k) | K852512 | THROMBO SCREEEN FIBRIN DEGRADATION PRODUCT KIT | GHH | 1985-09-17 | View |
| 510(k) | K834086 | CONTACT-K APTT REAGENT | GGN | 1984-02-03 | View |
| 510(k) | K820450 | THROMBOSCREEN | GIT | 1982-03-26 | View |
No matching devices.
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