K-number	K002240
Device name	RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0
Applicant	Precision Therapy Intl., Inc.
Product code	MUJ
Device class	Class II
Decision date	Aug 23, 2000
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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RENDER-PLAN 3-D 4.00 & PRECISE-PLAN 1.0

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