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MODIFICATIONS TO CORDIS' SUPER FLOW CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K862244
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
74 days

MODIFICATIONS TO CORDIS' SUPER FLOW CATHETERS

Page Type
Cleared 510(K)
510(k) Number
K862244
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1986
Days to Decision
74 days