# K212065: VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger

- Pathway: 510(k) (Traditional)
- Applicant: Remington Medical, Inc.
- Decided: Oct 7, 2021 after 97 days
- Product code: DPW (Flowmeter, Blood, Cardiovascular)
- Device class: 2
- Regulation: 21 CFR 870.2100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K082870 (2008). 1 ancestor in all.
3 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082870: Vti Intraoperative Doppler Systems, Vascular Technology Incorporated (2008) Summary page 4.

## Most influential descendants
- K241583: 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) (2024), 1 descendant of its own
- K260700: BlueDop Vascular Expert (2026), 0 descendants of its own
- K251904: 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) (2025), 0 descendants of its own

## Indications for use
The Remington Medical, Inc. VascuChek™ Clinical Device is intended for the non-invasive transcutaneous evaluation of blood flow in Peripheral Vasculature.

Source page: https://510kreport.com/device/K212065
Methodology: https://510kreport.com/methodology