K-number	K841923
Device name	DCX-100 CHEST UNIT-GL-5000M
Applicant	Transworld X-Ray Corp.
Product code	KPR
Device class	Class II
Decision date	Aug 10, 1984
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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DCX-100 CHEST UNIT-GL-5000M

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