Last synced on 12 October 2025 at 8:21 pm

ENDOCARDIAL SCREW-IN LEAD MODEL 1020T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895447
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1989
Days to Decision
103 days

ENDOCARDIAL SCREW-IN LEAD MODEL 1020T

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895447
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1989
Days to Decision
103 days