510(k) K875272 ยท DXK Echocardiograph
SONOLINE CF
| Applicant | Siemens Medical Laboratories, Inc., Pleasanton CA, US |
| Decision | Substantially Equivalent, Feb 18, 1988 |
| Received | Dec 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875272
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.