K-number	K102512
Device name	RMS SUBCUTANEOUS NEEDLE SET
Applicant	Repro-Med Systems, Inc.
Product code	FPA
Device class	Class II
Decision date	May 20, 2011
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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RMS SUBCUTANEOUS NEEDLE SET

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