510(k) K900002 ยท DXK Echocardiograph
DOPPLER OPTION FOR PLATINUM
| Applicant | Philips Medical Systems North America, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Apr 2, 1990 |
| Received | Jan 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900002
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.