510(k) K962424 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
NPB-4000
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, Dec 20, 1996 |
| Received | Jun 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962424
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.