K-number	K122298
Device name	AJEX 1200 H / AJEX 240H MOBILE X-RAY GENERATOR
Applicant	Ajex Meditech., Ltd.
Product code	IZL
Device class	Class II
Decision date	Mar 28, 2014
Decision	Substantially Equivalent
Regulation	892.1720

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View the full FDA submission: accessdata.fda.gov

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

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