Last synced on 25 January 2026 at 3:41 am

TYPE FH ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810494
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
164 days

TYPE FH ENDOCARDIAL LEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K810494
510(k) Type
Traditional
Applicant
BIOTRONIK SALES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1981
Days to Decision
164 days