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MEDTRONIC(R) GC III CORONARY GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K950179
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1995
Days to Decision
189 days
Submission Type
Statement

MEDTRONIC(R) GC III CORONARY GUIDING CATHETER

Page Type
Cleared 510(K)
510(k) Number
K950179
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/1995
Days to Decision
189 days
Submission Type
Statement