K-number	K950191
Device name	THE LOTECON PERSONAL CARE SYSTEM
Applicant	Lotecon, Inc.
Product code	FNM
Device class	Class II
Decision date	Jun 12, 1995
Decision	Substantially Equivalent
Regulation	880.5550

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View the full FDA submission: accessdata.fda.gov

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THE LOTECON PERSONAL CARE SYSTEM

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