510(k) K832050 ยท DPS Electrocardiograph
MORTARA INSTRUMENT #101
| Applicant | Mortara Instrument, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Dec 13, 1983 |
| Received | Jun 24, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832050
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.