K-number	K884626
Device name	MODIFIED SLIDING RECONSTITUTION DEVICE
Applicant	Baxter Healthcare Corp
Product code	LHI
Device class	Class II
Decision date	Nov 22, 1988
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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MODIFIED SLIDING RECONSTITUTION DEVICE

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