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Argus Cognitive ReVISION Software

Page Type
Cleared 510(K)
510(k) Number
K223322
510(k) Type
Traditional
Applicant
Argus Cognitive, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2023
Days to Decision
266 days
Submission Type
Summary

Argus Cognitive ReVISION Software

Page Type
Cleared 510(K)
510(k) Number
K223322
510(k) Type
Traditional
Applicant
Argus Cognitive, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2023
Days to Decision
266 days
Submission Type
Summary