Last synced on 23 May 2025 at 11:06 pm

VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211589
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2022
Days to Decision
248 days
Submission Type
Summary

VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Charger

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211589
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/2022
Days to Decision
248 days
Submission Type
Summary