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OARtrac System with Patient Specific Reusable Universal PSD Sensors

Page Type
Cleared 510(K)
510(k) Number
K162954
510(k) Type
Traditional
Applicant
RADIADYNE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2017
Days to Decision
220 days
Submission Type
Summary

OARtrac System with Patient Specific Reusable Universal PSD Sensors

Page Type
Cleared 510(K)
510(k) Number
K162954
510(k) Type
Traditional
Applicant
RADIADYNE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2017
Days to Decision
220 days
Submission Type
Summary