K-number	K913990
Device name	KTP/532 & KTP/YAG
Applicant	Laserscope
Product code	GEX
Device class	Class II
Decision date	Sep 2, 1992
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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KTP/532 & KTP/YAG

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