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RetinAI Discovery

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211715
510(k) Type
Traditional
Applicant
RetinAI Medical AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/28/2022
Days to Decision
329 days
Submission Type
Summary

RetinAI Discovery

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211715
510(k) Type
Traditional
Applicant
RetinAI Medical AG
Country
Switzerland
FDA Decision
Substantially Equivalent
Decision Date
4/28/2022
Days to Decision
329 days
Submission Type
Summary