510(k) K211589 ยท DPW Flowmeter, Blood, Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger
| Applicant | Remington Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Jan 27, 2022 |
| Received | May 24, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K211589
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.