FDA 510(k) Applications Submitted by BIOTEQUE CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K012526	08/06/2001	BIOTEQUE SCALP VEIN SET	BIOTEQUE CORP.
K992930	08/31/1999	BIOTEQUE HEMODIALYSIS BLOOD TUBING SET	BIOTEQUE CORP.
K993118	09/20/1999	BIOTEQUE A.V. FISTULA NEEDLE SET	BIOTEQUE CORP.
K002449	08/09/2000	BIOTEQ I.V. (INTRAVENOUS) SET	BIOTEQUE CORP.
K032292	07/24/2003	BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX	BIOTEQUE CORP.
K102633	09/13/2010	BIOTEQ ANGIOGRAPHIC CATHETER	BIOTEQUE CORP.
K033210	10/03/2003	BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET	BIOTEQUE CORP.
K013634	11/05/2001	BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK	BIOTEQUE CORP.
K150932	04/06/2015	Sheath Introducer	BIOTEQUE CORP.
K033862	12/12/2003	BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK	BIOTEQUE CORP.