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Rapid Aortic Measurements

Page Type
Cleared 510(K)
510(k) Number
K251987
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2025
Days to Decision
88 days
Submission Type
Summary

Rapid Aortic Measurements

Page Type
Cleared 510(K)
510(k) Number
K251987
510(k) Type
Traditional
Applicant
iSchemaView, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/2025
Days to Decision
88 days
Submission Type
Summary