FDA 510(k) Applications for Medical Device Product Code: FCF (Instrument, Biopsy, Mechanical, Gastrointestinal)

FDA 510(k) Applications for Medical Device Product Code "FCF"
(Instrument, Biopsy, Mechanical, Gastrointestinal)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K984168	UNITED STATES ENDOSCOPY GROUP, INC.	BARRETT'S ESOPHAGEAL CYTOLOGY DEVICE	12/07/1999
K062833	VIDACARE CORPORATION	POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM	11/30/2006
K070759	VIDACARE CORPORATION	POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM	05/21/2007