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CORDIS EXTREME PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992825
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1999
Days to Decision
23 days
Submission Type
Summary

CORDIS EXTREME PTA BALLOON CATHETER

Page Type
Cleared 510(K)
510(k) Number
K992825
510(k) Type
Special
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1999
Days to Decision
23 days
Submission Type
Summary