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Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard

Page Type
Cleared 510(K)
510(k) Number
K193360
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
29 days
Submission Type
Summary

Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard

Page Type
Cleared 510(K)
510(k) Number
K193360
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/2/2020
Days to Decision
29 days
Submission Type
Summary