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Universal SmartECG

Page Type
Cleared 510(K)
510(k) Number
K173952
510(k) Type
Traditional
Applicant
VectraCor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2018
Days to Decision
244 days
Submission Type
Summary

Universal SmartECG

Page Type
Cleared 510(K)
510(k) Number
K173952
510(k) Type
Traditional
Applicant
VectraCor, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2018
Days to Decision
244 days
Submission Type
Summary