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ACT III VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013705
510(k) Type
Traditional
Applicant
INNERSPACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2002
Days to Decision
305 days
Submission Type
Summary

ACT III VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K013705
510(k) Type
Traditional
Applicant
INNERSPACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2002
Days to Decision
305 days
Submission Type
Summary