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AcuityDRe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210919
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2021
Days to Decision
32 days
Submission Type
Summary

AcuityDRe

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210919
510(k) Type
Traditional
Applicant
Radmedix LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2021
Days to Decision
32 days
Submission Type
Summary