K-number	K895677
Device name	THE MURRAY MOBILIFT(TM)
Applicant	Medical/Surgical Specialties, Ltd.
Product code	FNG
Device class	Class II
Decision date	Oct 26, 1990
Decision	Substantially Equivalent
Regulation	880.5500

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View the full FDA submission: accessdata.fda.gov

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THE MURRAY MOBILIFT(TM)

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