K-number	K022411
Device name	PRECISEPLAN 2.0
Applicant	Precision Therapy Intl., Inc.
Product code	MUJ
Device class	Class II
Decision date	Sep 20, 2002
Decision	Substantially Equivalent
Regulation	892.5050

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Source

View the full FDA submission: accessdata.fda.gov

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PRECISEPLAN 2.0

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