K-number	K990406
Device name	KINGLI ACUPUNCTURE NEEDLE
Applicant	United Pacific Co., Ltd.
Product code	MQX
Device class	Class II
Decision date	Apr 16, 1999
Decision	Substantially Equivalent
Regulation	880.5580

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View the full FDA submission: accessdata.fda.gov

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KINGLI ACUPUNCTURE NEEDLE

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