510(k) K942685 ยท DXJ Display, Cathode-Ray Tube, Medical
ECG REVIEW STATION
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 12, 1997 |
| Received | Jun 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942685
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.