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AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122298
510(k) Type
Traditional
Applicant
Ajex Meditech., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2014
Days to Decision
605 days
Submission Type
Summary

AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122298
510(k) Type
Traditional
Applicant
Ajex Meditech., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2014
Days to Decision
605 days
Submission Type
Summary