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InvisionECG System

Page Type
Cleared 510(K)
510(k) Number
K143436
510(k) Type
Traditional
Applicant
InvisionHeart Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2015
Days to Decision
171 days
Submission Type
Summary

InvisionECG System

Page Type
Cleared 510(K)
510(k) Number
K143436
510(k) Type
Traditional
Applicant
InvisionHeart Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2015
Days to Decision
171 days
Submission Type
Summary