510(k) K904832 ยท DXK Echocardiograph
MODIFIED SYST: SONOS 500/1000 ULTRSOUND IMAG SYST
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Apr 22, 1991 |
| Received | Oct 23, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904832
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.