K-number	K042764
Device name	MEDLINE STRIDER MIDI 4
Applicant	Medline Industries, Inc.
Product code	INI
Device class	Class II
Decision date	Oct 8, 2004
Decision	Substantially Equivalent
Regulation	890.3800

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View the full FDA submission: accessdata.fda.gov

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MEDLINE STRIDER MIDI 4

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