K-number	K993385
Device name	AUTOJET 2 (NON-FIXED NEEDLE TYPE)
Applicant	Owen Mumford USA, Inc.
Product code	KZH
Device class	Class II
Decision date	Nov 10, 1999
Decision	Substantially Equivalent
Regulation	880.6920

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View the full FDA submission: accessdata.fda.gov

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AUTOJET 2 (NON-FIXED NEEDLE TYPE)

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