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CRITIVIEW, MODEL CRV3

Page Type
Cleared 510(K)
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)
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