# 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)

- Pathway: 510(k) (Special)
- Applicant: Remington Medical, Inc.
- Decided: Aug 30, 2024 after 88 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: 2 generations back to K082870 (2008). 3 ancestors in all.
1 later device descends from it; 1 cites 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)
- K211589: VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger, Remington Medical, Inc. (2022) Summary page 5.
- K212065: VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger, Remington Medical, Inc. (2021) Summary page 5.

## Most influential descendants
- 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
VascuChek® Kit, VascuChek® Transceiver, VascuChek® Clinical Probe, VascuChek® Charger: The VascuChek® device is intended for the non-invasive transcutaneous evaluation of blood flow in Peripheral Vasculature. VascuChek® Kit, VascuChek® Transceiver, VascuChek® Surgical Probe, VascuChek® Charger: The VascuChek® device is intended for the intraoperative and transcutaneous evaluation of blood flow in the following clinical applications: - Intraoperative (Microvascular and Vascular) - Intraoperative Neurological - Transrectal and Peripheral Vascular.

Source page: https://510kreport.com/device/K241583
Methodology: https://510kreport.com/methodology