K-number	K931839
Device name	ROTA SYSTEM XL
Applicant	Rota Systems Medfurniture, Inc.
Product code	HMF
Device class	Class I
Decision date	Nov 22, 1993
Decision	Substantially Equivalent
Regulation	886.1860

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View the full FDA submission: accessdata.fda.gov

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ROTA SYSTEM XL

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