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BIPOLAR PERNENOUS VENTRICULAR LEAD

Page Type
Cleared 510(K)
510(k) Number
K790344
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1979
Days to Decision
55 days

BIPOLAR PERNENOUS VENTRICULAR LEAD

Page Type
Cleared 510(K)
510(k) Number
K790344
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/17/1979
Days to Decision
55 days