K-number	K862002
Device name	MEDISYSTEMS PHERESIS NEEDLE
Applicant	Medisystems Corp.
Product code	FIE
Device class	Class II
Decision date	Jun 27, 1986
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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MEDISYSTEMS PHERESIS NEEDLE

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