K-number	K122837
Device name	AUTOJECT 2 FOR GLASSY SYRINGE
Applicant	Owen Mumford, Ltd.
Product code	KZH
Device class	Class II
Decision date	Oct 15, 2012
Decision	Substantially Equivalent
Regulation	880.6920

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View the full FDA submission: accessdata.fda.gov

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AUTOJECT 2 FOR GLASSY SYRINGE

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