Company ยท US
Medtronic Hemotec, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1996. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 20, 1996 | K954202 | PLATELET FUNCTION TEST ASSAY CARTRIDGES FOR THE HEPCON HMS Medtronic Hemotec, Inc. | JPA |
| Mar 24, 1995 | K944115 | HEPARIN ASSAY CARTRIDGES AND CONTROLS Medtronic Hemotec, Inc. | GFT |
| Sep 20, 1994 | K940426 | MEDTRONIC HEMOTEC ACT II AUTOMATED COAGULATION TIMER Medtronic Hemotec, Inc. | GKN |
| Sep 21, 1992 | K923594 | CLOTTRAC COAGULATION CONTROL Medtronic Hemotec, Inc. | JBP |
| Jul 21, 1992 | K922031 | HMS PURPLE AND BLACK HEPARIN CARTRIDGES & CONTROL Medtronic Hemotec, Inc. | JOX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||