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CARDIOPHONE

Page Type
Cleared 510(K)
510(k) Number
K781973
510(k) Type
Traditional
Applicant
NORTH AMERICAN MOTRONIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1979
Days to Decision
114 days

CARDIOPHONE

Page Type
Cleared 510(K)
510(k) Number
K781973
510(k) Type
Traditional
Applicant
NORTH AMERICAN MOTRONIC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1979
Days to Decision
114 days