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MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885240
510(k) Type
Traditional
Applicant
TPL-CORDIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
51 days

MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885240
510(k) Type
Traditional
Applicant
TPL-CORDIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/10/1989
Days to Decision
51 days