K-number	K832683
Device name	MONOJECT INJECTOMATIC
Applicant	Sherwood Medical Co.
Product code	KZH
Device class	Class II
Decision date	Sep 12, 1983
Decision	Substantially Equivalent
Regulation	880.6920

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Source

View the full FDA submission: accessdata.fda.gov

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MONOJECT INJECTOMATIC

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