510(k) K983928 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
KODAK HOME HEALTH MONITORING SYSTEM
| Applicant | Eastman Kodak Company, Rochester NY, US |
| Decision | Substantially Equivalent, Feb 11, 2000 |
| Received | Nov 5, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983928
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.