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ACS TORQUE DEVICE, ACS GUIDE WIRE INTRODUCER, ACS GUIDE WIRE ACCESSORY KITS

Page Type
Cleared 510(K)
510(k) Number
K950752
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1995
Days to Decision
87 days
Submission Type
Summary

ACS TORQUE DEVICE, ACS GUIDE WIRE INTRODUCER, ACS GUIDE WIRE ACCESSORY KITS

Page Type
Cleared 510(K)
510(k) Number
K950752
510(k) Type
Traditional
Applicant
ADVANCED CARDIOVASCULAR SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1995
Days to Decision
87 days
Submission Type
Summary