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ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852446
510(k) Type
Traditional
Applicant
DIAG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1985
Days to Decision
99 days

ENDOCARDIAL SCREW-IN LEAD WITH PLATINUM POROUS TIP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K852446
510(k) Type
Traditional
Applicant
DIAG CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1985
Days to Decision
99 days