510(k) K851496 ยท DXJ Display, Cathode-Ray Tube, Medical
ECG MONITOR MODEL RM102
| Applicant | Honeywell, Inc., Pleasantville NY, US |
| Decision | Substantially Equivalent, Jul 24, 1985 |
| Received | Apr 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851496
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.