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GUIDANT BALLOON CATHETER, SEVERAL MODELS

Page Type
Cleared 510(K)
510(k) Number
K021283
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2002
Days to Decision
14 days
Submission Type
Summary

GUIDANT BALLOON CATHETER, SEVERAL MODELS

Page Type
Cleared 510(K)
510(k) Number
K021283
510(k) Type
Traditional
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2002
Days to Decision
14 days
Submission Type
Summary