K-number	K911257
Device name	MR-5200 FULL DISCLOSURE SYSTEM
Applicant	Mennen Medical, Inc.
Product code	DSH
Device class	Class II
Decision date	Aug 19, 1991
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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MR-5200 FULL DISCLOSURE SYSTEM

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