K-number	K121390
Device name	LUBE JELLY SURINGE
Applicant	Nurse Assist, Inc.
Product code	KMJ
Device class	Class I
Decision date	Aug 10, 2012
Decision	Substantially Equivalent
Regulation	880.6375

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Source

View the full FDA submission: accessdata.fda.gov

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LUBE JELLY SURINGE

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