510(k) K861023 ยท DPW Flowmeter, Blood, Cardiovascular
DOPPLEX, PULSED/CONTINUOUS WAVE DOPPOLER
| Applicant | Diagnostic Electronics Corp., Lexington MA, US |
| Decision | Substantially Equivalent, Nov 17, 1986 |
| Received | Mar 18, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861023
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.