510(k) K926226 ยท DTZ Oxygenator, Cardiopulmonary Bypass
INTERSEPT FILTERED CARDIOTOMY RESERVOIR
| Applicant | Medtronic Vascular, Anaheim CA, US |
| Decision | Substantially Equivalent, Jun 22, 1993 |
| Received | Dec 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926226
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 26, 2007 | Medtronic Perfusion Systems Medtronic Intersept Filtered Cardiotomy Reservoir, Model 1351, Non-pyrogenic, Sterile, Manufacturer: Medtronic, Inc., Minneapolis, MN Terminated |
DTZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.