K-number	K901638
Device name	MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33
Applicant	Lasermatic, Inc.
Product code	GEX
Device class	Class II
Decision date	Jun 27, 1990
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33

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