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Lunit INSIGHT CXR Triage

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211733
510(k) Type
Traditional
Applicant
Lunit Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
159 days
Submission Type
Summary

Lunit INSIGHT CXR Triage

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211733
510(k) Type
Traditional
Applicant
Lunit Inc.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
159 days
Submission Type
Summary