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ENDOCARDIAL BIPOLAR LEAD

Page Type
Cleared 510(K)
510(k) Number
K781456
510(k) Type
Traditional
Applicant
AMERICAN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1978
Days to Decision
103 days

ENDOCARDIAL BIPOLAR LEAD

Page Type
Cleared 510(K)
510(k) Number
K781456
510(k) Type
Traditional
Applicant
AMERICAN TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/4/1978
Days to Decision
103 days