510(k) K920377 ยท LOS
MORTARA INSTRUMENT MODEL ECG PREVU
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 28, 1992 |
| Received | Jan 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920377
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.