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CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031629
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2003
Days to Decision
10 days
Submission Type
Summary

CANON NON-MYDRIATIC RETINAL CAMERA, MODEL CR-DGI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031629
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2003
Days to Decision
10 days
Submission Type
Summary