K-number	K092023
Device name	NAVIJECT SUB2-1P, MODEL: LP604430
Applicant	Medicel AG
Product code	MSS
Device class	Class I
Decision date	Jul 28, 2009
Decision	Substantially Equivalent
Regulation	886.4300

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View the full FDA submission: accessdata.fda.gov

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NAVIJECT SUB2-1P, MODEL: LP604430

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