510(k) K873214 ยท DPT Probe, Blood-Flow, Extravascular
APX CARDIO ECHOCARDIOGRAPHY SYSTEM #H4300
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 1, 1988 |
| Received | Aug 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873214
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.