K-number	K150698
Device name	Gemini Sterilization Wrap
Applicant	Medline Industries, Inc.
Product code	FRG
Device class	Class II
Decision date	Nov 20, 2015
Decision	Substantially Equivalent
Regulation	880.6850

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Source

View the full FDA submission: accessdata.fda.gov

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Gemini Sterilization Wrap

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