510(k) K212065 ยท DPW Flowmeter, Blood, Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger
| Applicant | Remington Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Oct 7, 2021 |
| Received | Jul 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212065
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.