K-number	K923744
Device name	CIDEX PLUS 28 DAY SOLUTION
Applicant	Johnson & Johnson Medical, Inc.
Product code	LRJ
Device class	Class I
Decision date	Mar 29, 1994
Decision	Substantially Equivalent
Regulation	880.6890

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View the full FDA submission: accessdata.fda.gov

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CIDEX PLUS 28 DAY SOLUTION

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