Medtronic Hemotec, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K954202 | PLATELET FUNCTION TEST ASSAY CARTRIDGES FOR THE HEPCON HMS | June 20, 1996 |
| K944115 | HEPARIN ASSAY CARTRIDGES AND CONTROLS | March 24, 1995 |
| K940426 | MEDTRONIC HEMOTEC ACT II AUTOMATED COAGULATION TIMER | September 20, 1994 |
| K923594 | CLOTTRAC COAGULATION CONTROL | September 21, 1992 |
| K922031 | HMS PURPLE AND BLACK HEPARIN CARTRIDGES & CONTROL | July 21, 1992 |