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ENDOCARDIAL BIPOLAR LEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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