K-number	K900857
Device name	NON STERILE PARENTERAL SUPPLY KIT
Applicant	Intermed, Inc.
Product code	FMF
Device class	Class II
Decision date	May 22, 1990
Decision	Substantially Equivalent — Kit Device
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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NON STERILE PARENTERAL SUPPLY KIT

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