K-number	K881993
Device name	PXI (PERSONAL X-RAY IMAGER) 512
Applicant	Oklahoma Digital Technologies, Inc.
Product code	LLZ
Device class	Class II
Decision date	Sep 19, 1988
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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PXI (PERSONAL X-RAY IMAGER) 512

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