HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX (K893133) — FDA 510(k) Clearance | Predicase

K-number	K893133
Device name	HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX
Applicant	Mennen Medical, Inc.
Product code	KLK
Device class	Class II
Decision date	Jul 14, 1989
Decision	Substantially Equivalent
Regulation	868.2500

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View the full FDA submission: accessdata.fda.gov

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