K-number	K780947
Device name	510 BEDSIDE X-RAY SYSTEM
Applicant	Union Carbide Corp.
Product code	IZL
Device class	Class II
Decision date	Jun 22, 1978
Decision	Substantially Equivalent
Regulation	892.1720

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View the full FDA submission: accessdata.fda.gov

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510 BEDSIDE X-RAY SYSTEM

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