Last synced on 14 November 2025 at 11:06 pm

IMPLANTABLE ENDOCARDIAL SCREW-IN ELEC

Page Type
Cleared 510(K)
510(k) Number
K791732
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1979
Days to Decision
14 days

IMPLANTABLE ENDOCARDIAL SCREW-IN ELEC

Page Type
Cleared 510(K)
510(k) Number
K791732
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/1979
Days to Decision
14 days