510(k) K800553 ยท DXK Echocardiograph
ULTRA IMAGER
| Applicant | Honeywell, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 21, 1980 |
| Received | Mar 11, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800553
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.