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GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300

Page Type
Cleared 510(K)
510(k) Number
K001969
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2000
Days to Decision
49 days
Submission Type
Summary

GT2 FUSION GUIDE WIRE, MODEL NTLHLJ180,NTLHLS180, NTLHLJ300, NTLHLS300

Page Type
Cleared 510(K)
510(k) Number
K001969
510(k) Type
Special
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2000
Days to Decision
49 days
Submission Type
Summary