Last synced on 19 July 2024 at 11:05 pm

DIGITAL RADIOGRAPHY MODEL CXDI-40EG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050987
510(k) Type
Traditional
Applicant
CANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2005
Days to Decision
8 days
Submission Type
Summary

DIGITAL RADIOGRAPHY MODEL CXDI-40EG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K050987
510(k) Type
Traditional
Applicant
CANON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2005
Days to Decision
8 days
Submission Type
Summary