510(k) K970182 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
DINAMAP COMPACT MONITOR
| Applicant | Johnson & Johnson Medical, Inc., Tampa FL, US |
| Decision | Substantially Equivalent, Aug 18, 1997 |
| Received | Jan 17, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970182
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.