K-number	K072454
Device name	INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS
Applicant	Integra Radionics, Inc.
Product code	IYE
Device class	Class II
Decision date	Oct 16, 2007
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS

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