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AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4

Page Type
Cleared 510(K)
510(k) Number
K231709
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2023
Days to Decision
30 days
Submission Type
Summary

AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4

Page Type
Cleared 510(K)
510(k) Number
K231709
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2023
Days to Decision
30 days
Submission Type
Summary