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ECG SERIES ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K111805
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2011
Days to Decision
58 days
Submission Type
Summary

ECG SERIES ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K111805
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/24/2011
Days to Decision
58 days
Submission Type
Summary