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DIGITAL RADIOGRAPHY CXDI-40G COMPACT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090623
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2009
Days to Decision
15 days
Submission Type
Summary

DIGITAL RADIOGRAPHY CXDI-40G COMPACT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K090623
510(k) Type
Traditional
Applicant
CANON U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2009
Days to Decision
15 days
Submission Type
Summary