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EXPANSION OF THE CORDIS PTA DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K894899
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
178 days

EXPANSION OF THE CORDIS PTA DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K894899
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
178 days