510(k) K920333 ยท DPW Flowmeter, Blood, Cardiovascular
SMARTDOP 20 BI-DIRECTIONAL BLOOD FLOW DETECTOR
| Applicant | Koven and Assoc., Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jan 22, 1993 |
| Received | Jan 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920333
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.