K-number	K140369
Device name	MEDLINE NEURO SPONGE
Applicant	Medline Industries, Inc.
Product code	HBA
Device class	Class II
Decision date	Sep 26, 2014
Decision	Substantially Equivalent
Regulation	882.4700

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View the full FDA submission: accessdata.fda.gov

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MEDLINE NEURO SPONGE

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