K-number	K893787
Device name	LIFECELL RECOVERY CONTAINER
Applicant	Baxter Healthcare Corp
Product code	KJF
Device class	Class I
Decision date	Jun 23, 1989
Decision	Substantially Equivalent
Regulation	864.2240

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View the full FDA submission: accessdata.fda.gov

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LIFECELL RECOVERY CONTAINER

Everything you need for a 510(k) submission. Nothing you don't.