510(k) K130208 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
BERNOULLI ENTERPRISE SOFTWARE
| Applicant | Cardiopulmonary Corp., Milford CT, US |
| Decision | Substantially Equivalent, Dec 20, 2013 |
| Received | Jan 28, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130208
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.