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QUIX DIGITAL RADIOGRAPHIC UPGRADE

Page Type
Cleared 510(K)
510(k) Number
K052661
510(k) Type
Traditional
Applicant
EDGE MEDICAL DEVICES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/7/2006
Days to Decision
253 days
Submission Type
Summary

QUIX DIGITAL RADIOGRAPHIC UPGRADE

Page Type
Cleared 510(K)
510(k) Number
K052661
510(k) Type
Traditional
Applicant
EDGE MEDICAL DEVICES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/7/2006
Days to Decision
253 days
Submission Type
Summary