510(k) K942613 ยท DPW Flowmeter, Blood, Cardiovascular
SMARTDOP 30 BI-DIRECTIONAL BLOOD FLOW DETECTOR
| Applicant | Koven Technology, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 23, 1994 |
| Received | Jun 2, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942613
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.