K-number	K160857
Device name	HF 718BD X-Ray System
Applicant	Arquilla, Inc. Dba X-Cel X-Ray Corporation
Product code	KPR
Device class	Class II
Decision date	Feb 24, 2017
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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HF 718BD X-Ray System

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