Last synced on 25 January 2026 at 3:41 am

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)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251904
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2025
Days to Decision
153 days
Submission Type
Summary

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)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K251904
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2025
Days to Decision
153 days
Submission Type
Summary