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CORDIS ANCOR ACTIVE FIXATION LEAD

Page Type
Cleared 510(K)
510(k) Number
K832422
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1986
Days to Decision
1110 days

CORDIS ANCOR ACTIVE FIXATION LEAD

Page Type
Cleared 510(K)
510(k) Number
K832422
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/1986
Days to Decision
1110 days