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DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093816
510(k) Type
Traditional
Applicant
MEDIEN INTERNATIONAL CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
298 days
Submission Type
Summary

DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093816
510(k) Type
Traditional
Applicant
MEDIEN INTERNATIONAL CO., LTD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
298 days
Submission Type
Summary