510(k) K871555 ยท DXK Echocardiograph
RT5000 W/QUANTI. SPEC. DOPPLER, CW DOPP. MODIFICA.
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Mar 2, 1988 |
| Received | Apr 22, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871555
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.