510(k) K010452 ยท DPW Flowmeter, Blood, Cardiovascular
BI-DIRECTIONAL DOPPLER VOLUME FLOWMETER, MODEL DVM-4300 & 4300T
| Applicant | Koven Technology, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Feb 15, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010452
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.