K-number	K902157
Device name	JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR
Applicant	Johnson & Johnson Medical, Inc.
Product code	FMF
Device class	Class II
Decision date	Nov 29, 1990
Decision	Unknown
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR

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