K-number	K860113
Device name	DOUBLE-JECT TRANSFER NEEDLE
Applicant	Medimix Products, Inc.
Product code	LHI
Device class	Class II
Decision date	Feb 12, 1986
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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DOUBLE-JECT TRANSFER NEEDLE

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