510(k) K896613 ยท DPW Flowmeter, Blood, Cardiovascular
FLAT VASCULAR PROBE
| Applicant | Imex Medical Systems, Inc., Golden CO, US |
| Decision | Substantially Equivalent, Feb 16, 1990 |
| Received | Nov 21, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896613
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.