510(k) K061675 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
VISION VXC CENTRAL STATION, MODEL 4300
| Applicant | Invivo Corporation, Orlando FL, US |
| Decision | Substantially Equivalent, Aug 2, 2006 |
| Received | Jun 14, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061675
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.