K-number	K833122
Device name	BURLINGTON ANTIMICROBIAL STOCKINEETTE
Applicant	Balfour, Inc.
Product code	KKX
Device class	Class II
Decision date	Jan 25, 1984
Decision	Substantially Equivalent
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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BURLINGTON ANTIMICROBIAL STOCKINEETTE

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