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MODIFIED MODEL 5401B TEST CABLE

Page Type
Cleared 510(K)
510(k) Number
K900622
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1990
Days to Decision
77 days

MODIFIED MODEL 5401B TEST CABLE

Page Type
Cleared 510(K)
510(k) Number
K900622
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1990
Days to Decision
77 days