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In this section: Substantially Equivalent 510(k) Device Information

Revised 510(k) Documents from Archived Content

This list contains revised 510(k) documents from archived content.

510(k) Number	Applicant	Device Name	Decision Date
BK120046	Diagnostic Grifols, S.A.	DG THERM	7/19/2013
BK080057	Kaylight Corporation	MyCells Autologous Platelet Preparation Kit	9/24/2009
BK090010	Ljungberg & Kogel AB	Biomizer BM330 with XBee (Wireless) Option	7/17/2009

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