K-number	K853900
Device name	ENDO-LASE CD40 FOR NEUROSURGERY
Applicant	Endo Lase, Inc.
Product code	GEX
Device class	Class II
Decision date	Jun 18, 1986
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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ENDO-LASE CD40 FOR NEUROSURGERY

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