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CORDIS DUCOR PERCUT. TRANS. ANGIO. CATH.

Page Type
Cleared 510(K)
510(k) Number
K812168
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1981
Days to Decision
32 days

CORDIS DUCOR PERCUT. TRANS. ANGIO. CATH.

Page Type
Cleared 510(K)
510(k) Number
K812168
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/1981
Days to Decision
32 days