K-number	K880726
Device name	JMS APHERESIS NEEDLE
Applicant	Jms Co., Ltd.
Product code	FIE
Device class	Class II
Decision date	Mar 16, 1988
Decision	Substantially Equivalent
Regulation	876.5540

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Source

View the full FDA submission: accessdata.fda.gov

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JMS APHERESIS NEEDLE

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