K-number	K942207
Device name	REFLEX INS INSUFFLATION NEEDLE
Applicant	Richard-Allan Medical
Product code	HIF
Device class	Class II
Decision date	May 27, 1994
Decision	Substantially Equivalent
Regulation	884.1730

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View the full FDA submission: accessdata.fda.gov

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REFLEX INS INSUFFLATION NEEDLE

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