510(k) K024278 ยท DPS Electrocardiograph
PACEART SYSTEM
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, May 29, 2003 |
| Received | Dec 23, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K024278
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 6, 2007 | Medtronic Inc. Cardiac Rhythm Managment Medtronic Paceart System, 2006 Edition, Medtronic, Inc. 710 Medtronic Parkway, Minneapolis, MN 55432-5604 USA. The Paceart System can act as a Practice Management software application and is intende Terminated |
DPS | None listed |
| May 31, 2006 | Medtronic Inc. Cardiac Rhythm Managment Medtronic Paceart 2004 Second Edition & Paceart 2005 First Edition versions of the Paceart Gateway Software. The Medtronic Paceart System is a personal computer based pacemaker-testing system, a 12-l Terminated |
DPS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.