K-number	K791660
Device name	PREPACELL-BONE MARROW SAMPLER
Applicant	Applied Medical Devices, Inc.
Product code	FMF
Device class	Class II
Decision date	Sep 12, 1979
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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PREPACELL-BONE MARROW SAMPLER

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