HORIZON 2000/S 266-XXX-XXX (K880595) — FDA 510(k) Clearance | Predicase

K-number	K880595
Device name	HORIZON 2000/S 266-XXX-XXX
Applicant	Mennen Medical, Inc.
Product code	DPS
Device class	Class II
Decision date	May 6, 1988
Decision	Substantially Equivalent
Regulation	870.2340

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View the full FDA submission: accessdata.fda.gov

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