Last synced on 23 May 2025 at 11:06 pm

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)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241583
510(k) Type
Special
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2024
Days to Decision
88 days
Submission Type
Summary

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)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241583
510(k) Type
Special
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/2024
Days to Decision
88 days
Submission Type
Summary