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CENTERVUE DIGITAL RETINOGRAPHY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101935
510(k) Type
Traditional
Applicant
CENTERVUE SPA
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/27/2010
Days to Decision
107 days
Submission Type
Summary

CENTERVUE DIGITAL RETINOGRAPHY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101935
510(k) Type
Traditional
Applicant
CENTERVUE SPA
Country
Italy
FDA Decision
Substantially Equivalent
Decision Date
10/27/2010
Days to Decision
107 days
Submission Type
Summary