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VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212065
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2021
Days to Decision
97 days
Submission Type
Summary

VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212065
510(k) Type
Traditional
Applicant
Remington Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2021
Days to Decision
97 days
Submission Type
Summary