Company ยท US
Med-West, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1988. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FIQ | Cannula, A-V Shunt | 2 |
| LFK | Catheter, Femoral | 2 |
| DRE | Dilator, Vessel, For Percutaneous Catheterization | 1 |
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | 1 |
| DXT | Injector And Syringe, Angiographic | 1 |
| INO | Chair, Positioning, Electric | 1 |
| LFJ | Catheter, Subclavian | 1 |
| NAD | Dressing, Wound, Occlusive | 1 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 31, 1988 | K880877 | CONTRAST INJECTION DEVICE Med-West, Inc. | DXT |
| Mar 17, 1988 | K880398 | POWER TOILET ELEVATOR Med-West, Inc. | INO |
| Dec 18, 1987 | K874470 | MWI 400 WOUND DRESSING Med-West, Inc. | NAD |
| Sep 15, 1987 | K872724 | SHEATH/DILATORS Med-West, Inc. | DRE |
| Jan 3, 1986 | K854612 | ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 Med-West, Inc. | LFK |
| Jun 12, 1985 | K852162 | MNI 400 INJECTION CAPS Med-West, Inc. | LFJ |
| Jun 14, 1984 | K842342 | MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN Med-West, Inc. | |
| Aug 12, 1983 | K832124 | CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI Med-West, Inc. | DWF |
| Jul 7, 1983 | K831828 | TEFLON FEMORAL CATHETER MWI 100,10 & Med-West, Inc. | LFK |
| Jun 3, 1983 | K831440 | SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 Med-West, Inc. | FIQ |
| Jun 3, 1983 | K831401 | SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS Med-West, Inc. | FIQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||