Bioteque Corp.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K150932 | Sheath Introducer | DRE | 2016-07-22 | View |
| 510(k) | K102633 | BIOTEQ ANGIOGRAPHIC CATHETER | DQO | 2011-09-09 | View |
| 510(k) | K033862 | BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK | FGE | 2005-02-14 | View |
| 510(k) | K033210 | BIOTEQ DOUBLE PIGTAIL URETERAL STENT SET | FAD | 2004-12-30 | View |
| 510(k) | K032292 | BIOTEQUE A.V. FISTULA NEEDLE SET WITH SAFETY FLEX | FOZ | 2004-03-22 | View |
| 510(k) | K013634 | BIOTEQUE 3 IN 1 HEMODIALYSIS BLOOD TUBING PACK | FJK | 2002-07-09 | View |
| 510(k) | K012526 | BIOTEQUE SCALP VEIN SET | FPA | 2001-09-14 | View |
| 510(k) | K002449 | BIOTEQ I.V. (INTRAVENOUS) SET | FPA | 2000-12-22 | View |
| 510(k) | K992930 | BIOTEQUE HEMODIALYSIS BLOOD TUBING SET | FJK | 2000-02-09 | View |
| 510(k) | K993118 | BIOTEQUE A.V. FISTULA NEEDLE SET | FIE | 1999-12-17 | View |
| 510(k) | K915491 | CURELLE | HHK | 1992-11-04 | View |
No matching devices.
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