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CENTERVUE DIGITAL RETINOGRAPHY SYSTEM

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