Last synced on 20 December 2024 at 11:05 pm

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