K-number	K072682
Device name	50W CERALAS D 1950NM DIODE LASER
Applicant	Biolitec, Inc.
Product code	GEX
Device class	Class II
Decision date	Apr 18, 2008
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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50W CERALAS D 1950NM DIODE LASER

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