FDA 510(k) Applications for Medical Device Product Code: FCK (Instrument, Biopsy, Suction)

FDA 510(k) Applications for Medical Device Product Code "FCK"
(Instrument, Biopsy, Suction)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K062159	AUS SYSTEMS PTY LTD.	RB12 SUCTION RECTAL BIOPSY SYSTEM	09/05/2006
K061201	UNITED STATES ENDOSCOPY GROUP, INC.	DSNARE DIMINUTIVE POLYPECTOMY AND SUCTION SYSTEM, MODEL 00711087	05/30/2006
K051637	UNITED STATES ENDOSCOPY GROUP, INC.	DSNARE, MODEL 00711087	10/31/2005
K103326	UNITED STATES ENDOSCOPY GROUP, INC.	MULTIPLE BIOPSY SYSTEM	04/06/2011
K153763	WILSON-COOK MEDICAL, INC.	Howell Biliary Aspiration Needle	04/06/2017