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TEMPORARY PERVENOUS J-ATRIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K812781
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1981
Days to Decision
24 days

TEMPORARY PERVENOUS J-ATRIAL LEAD

Page Type
Cleared 510(K)
510(k) Number
K812781
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/1981
Days to Decision
24 days