Last synced on 14 November 2025 at 11:06 pm

ACUITY BREAK-AWAY GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093969
510(k) Type
Special
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2010
Days to Decision
72 days
Submission Type
Summary

ACUITY BREAK-AWAY GUIDE CATHETER

Page Type
Cleared 510(K)
510(k) Number
K093969
510(k) Type
Special
Applicant
CARDIAC PACEMAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/2010
Days to Decision
72 days
Submission Type
Summary