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THE GUIDER CORONARY GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K903216
510(k) Type
Traditional
Applicant
INTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1990
Days to Decision
88 days

THE GUIDER CORONARY GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K903216
510(k) Type
Traditional
Applicant
INTEC MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/1990
Days to Decision
88 days