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CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL

Page Type
Cleared 510(K)
510(k) Number
K811539
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1981
Days to Decision
30 days

CORDIS ENCOR PEWENOUS VENTRICULAR BIPOL

Page Type
Cleared 510(K)
510(k) Number
K811539
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1981
Days to Decision
30 days