510(k) K050951 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone
MEDSTAR 220, MODEL 533-220; MEDSTAR 230, MODEL 533-230; MEDSTAR 360, MODEL 533-360; MEDSTAR 370, MODEL 533-370
| Applicant | Cibernet Systems Corp., Ann Arbor MI, US |
| Decision | Substantially Equivalent, Jul 19, 2005 |
| Received | Apr 15, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050951
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 25, 2010 | Cybernet Systems Corp. Cybernet Medical MedStar Telemedicine System, Manufactured by Cybernet Medical, Ann Arbor, MI; Model 533-210.
The device is for a remote medical data collection device for the monitoring of patien Terminated |
DXH | None listed |
| Feb 25, 2010 | Cybernet Systems Corp. Cybernet Medical MedStar Telemedicine System, Manufactured by Cybernet Medical, Ann Arbor, MI; Model 533-380.
The device is for a remote medical data collection device for the monitoring of patient Terminated |
DXH | None listed |
| Feb 25, 2010 | Cybernet Systems Corp. Cybernet Medical MedStar Telemedicine System, Manufactured by Cybernet Medical, Ann Arbor, MI; Model 533-386.
The device is for a remote medical data collection device for the monitoring of patien Terminated |
DXH | None listed |
| Feb 25, 2010 | Cybernet Systems Corp. Cybernet Medical MedStar Telemedicine System, Manufactured by Cybernet Medical, Ann Arbor, MI; Model 533-381.
The device is for a remote medical data collection device for the monitoring of patient Terminated |
DXH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.