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VIKING OPTIMA GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K001435
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2000
Days to Decision
25 days
Submission Type
Summary

VIKING OPTIMA GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K001435
510(k) Type
Special
Applicant
GUIDANT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2000
Days to Decision
25 days
Submission Type
Summary