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CORDIS FLOW DIRECTED BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K801865
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1980
Days to Decision
15 days

CORDIS FLOW DIRECTED BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K801865
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1980
Days to Decision
15 days