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PRIME ECG SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030104
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2003
Days to Decision
149 days
Submission Type
Summary

PRIME ECG SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030104
510(k) Type
Traditional
Applicant
MERIDIAN MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2003
Days to Decision
149 days
Submission Type
Summary