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CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K993720
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
76 days
Submission Type
Summary

CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K993720
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2000
Days to Decision
76 days
Submission Type
Summary