510(k) K241583 ยท DPW Flowmeter, Blood, Cardiovascular
VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-CP-01, VC-CH-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger (VC-KIT-01, VC-TRX-01, VC-SP-01, VC-CH-01)
| Applicant | Remington Medical, Inc., Alpharetta GA, US |
| Decision | Substantially Equivalent, Aug 30, 2024 |
| Received | Jun 3, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K241583
No recall in the FDA data names this 510(k).
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