Last synced on 25 January 2026 at 3:41 am

CRITIVIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051145
510(k) Type
Traditional
Applicant
Critisense , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
259 days
Submission Type
Summary

CRITIVIEW

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051145
510(k) Type
Traditional
Applicant
Critisense , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
259 days
Submission Type
Summary