K-number	K061025
Device name	ACCUTECH ENDOLITE PROBE
Applicant	Accutech Medical Technologies, Inc.
Product code	FFS
Device class	Class II
Decision date	May 31, 2006
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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ACCUTECH ENDOLITE PROBE

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