K-number	K081355
Device name	BIOFLEX LD-R100 TREATMENT HEAD
Applicant	Meditech International, Inc.
Product code	ILY
Device class	Class II
Decision date	Dec 18, 2008
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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BIOFLEX LD-R100 TREATMENT HEAD

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