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ACT II ICP MONITORING SYSTEM AND VENTRICULAR CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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