K-number	K761339
Device name	RADIAL TRAVEL SPEC. PROCEDURES TABLE
Applicant	Xre Corp.
Product code	IZZ
Device class	Class II
Decision date	Jan 5, 1977
Decision	Substantially Equivalent
Regulation	892.1980

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View the full FDA submission: accessdata.fda.gov

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RADIAL TRAVEL SPEC. PROCEDURES TABLE

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