510(k) K873032 ยท DXK Echocardiograph
GENESIS II, 2.5/5.0 MHZ S.E/5.0MHZ/3.5 16/19 MM AN
| Applicant | Biosound, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Feb 18, 1988 |
| Received | Aug 4, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873032
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.