K-number	K031828
Device name	NATURALASE LP ND:YAG LASER
Applicant	Focus Medical, LLC
Product code	GEN
Device class	Class I
Decision date	Jul 17, 2003
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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NATURALASE LP ND:YAG LASER

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