K-number	K011669
Device name	BW ACUPUNCTURE NEEDLES
Applicant	H F Intl. Co.
Product code	MQX
Device class	Class II
Decision date	Jul 9, 2001
Decision	Substantially Equivalent
Regulation	880.5580

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View the full FDA submission: accessdata.fda.gov

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BW ACUPUNCTURE NEEDLES

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