510(k) K913209 ยท DXK Echocardiograph
ACCESSORY TO GENESIS III (GCFM)
| Applicant | Biosound, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, May 15, 1992 |
| Received | Jul 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913209
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.