Bioteque Corp.
Bioteque Corp. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2016.
Top product codes for Bioteque Corp.
Recent clearances by Bioteque Corp.
- K150932 — Sheath Introducer
- K102633 — BIOTEQ ANGIOGRAPHIC CATHETER
- K033862 — BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
- K033210 — BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET
- K032292 — BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX
- K013634 — BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK
- K012526 — BIOTEQUE SCALP VEIN SET
- K002449 — BIOTEQ I.V. (INTRAVENOUS) SET
- K992930 — BIOTEQUE HEMODIALYSIS BLOOD TUBING SET
- K993118 — BIOTEQUE A.V. FISTULA NEEDLE SET
- K915491 — CURELLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.