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CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800

Page Type
Cleared 510(K)
510(k) Number
K992703
510(k) Type
Traditional
Applicant
Premier Heart, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
222 days
Submission Type
Summary

CARDIOTRON EKG MULTI-PHASE INFORMATION ANALYSIS SYSTEM, MODELS 3800, 6800, 8800

Page Type
Cleared 510(K)
510(k) Number
K992703
510(k) Type
Traditional
Applicant
Premier Heart, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
222 days
Submission Type
Summary