K-number	K952518
Device name	SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE
Applicant	Medi-Dose, Inc.
Product code	FMI
Device class	Class II
Decision date	Jul 28, 1995
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE

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