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QUIX DIGITAL RADIOGRAPHIC UPGRADE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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