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CRITIVIEW, MODEL CRV3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062977
510(k) Type
Traditional
Applicant
CRITISENSE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2007
Days to Decision
152 days
Submission Type
Summary

CRITIVIEW, MODEL CRV3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062977
510(k) Type
Traditional
Applicant
CRITISENSE LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2007
Days to Decision
152 days
Submission Type
Summary