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ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K010422
510(k) Type
Traditional
Applicant
INNERSPACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2001
Days to Decision
136 days
Submission Type
Summary

ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER

Page Type
Cleared 510(K)
510(k) Number
K010422
510(k) Type
Traditional
Applicant
INNERSPACE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/2001
Days to Decision
136 days
Submission Type
Summary