Last synced on 25 January 2026 at 3:41 am

IMPLANTABLE ENDOCARDIAL SCREW-IN ELEC

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