510(k) K251904 ยท DPW Flowmeter, Blood, Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01)
| Applicant | Remington Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Nov 20, 2025 |
| Received | Jun 20, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251904
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.