Bioteque Corp. is one of 4771 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioteque Corp. - FDA 510(k) Cleared Devices
11
Total
10
Cleared
0
Denied
Bioteque Corp. has 10 FDA 510(k) cleared medical devices. Based in Levittown, US.
Historical record: 10 cleared submissions from 1992 to 2016. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Bioteque Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioteque Corp.
11 devices
Cleared
Jul 22, 2016
Sheath Introducer
Cardiovascular
473d
Cleared
Sep 09, 2011
BIOTEQ ANGIOGRAPHIC CATHETER
Cardiovascular
361d
Cleared
Feb 14, 2005
BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY...
Gastroenterology & Urology
430d
Cleared
Dec 30, 2004
BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET
Gastroenterology & Urology
454d
Cleared
Mar 22, 2004
BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX
General Hospital
242d
Cleared
Jul 09, 2002
BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
Gastroenterology & Urology
246d
Cleared
Sep 14, 2001
BIOTEQUE SCALP VEIN SET
General Hospital
39d
Cleared
Dec 22, 2000
BIOTEQ I.V. (INTRAVENOUS) SET
General Hospital
135d
Cleared
Feb 09, 2000
BIOTEQUE HEMODIALYSIS BLOOD TUBING SET
Gastroenterology & Urology
162d
Cleared
Dec 17, 1999
BIOTEQUE A.V. FISTULA NEEDLE SET
Gastroenterology & Urology
88d
Cleared
Nov 04, 1992
CURELLE
Obstetrics & Gynecology
334d