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

BK080057 - MyCells Autologous Platelet Preparation Kit

510(k) Number: BK080057
Applicant: Kaylight Corporation
Device Name: MyCells Autologous Platelet Preparation Kit
Decision Date: 9/24/2009

Supporting Documents

BK080057 Letter
The original SE letter has been replaced with a revised SE letter to revise the product code.

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