510(k) K894370 ยท DXK Echocardiograph
GENESIS III, (MOD. 7003/7004)
| Applicant | Biosound, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Jan 29, 1990 |
| Received | Jul 14, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894370
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.