510(k) K201114 ยท DPW Flowmeter, Blood, Cardiovascular
Bidop 7
| Applicant | Koven Technology, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jan 5, 2021 |
| Received | Apr 27, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201114
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.