Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Med-West with 11 510(k) clearances. The most recent is a 510(k) clearance dated May 31, 1988: CONTRAST INJECTION DEVICE.
| May 31, 1988 | CONTRAST INJECTION DEVICEK880877 · DXT | 510(k) clearances |
| Mar 17, 1988 | POWER TOILET ELEVATORK880398 · INO | 510(k) clearances |
| Dec 18, 1987 | MWI 400 WOUND DRESSINGK874470 · NAD | 510(k) clearances |
| Sep 15, 1987 | SHEATH/DILATORSK872724 · DRE | 510(k) clearances |
| Jan 3, 1986 | ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7K854612 · LFK | 510(k) clearances |
| Jun 12, 1985 | MNI 400 INJECTION CAPSK852162 · LFJ | 510(k) clearances |
| Jun 14, 1984 | MWI 888 & 666 DOUBLE LUMEN SUBCLAVIANK842342 · | 510(k) clearances |
| Aug 12, 1983 | CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPIK832124 · DWF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
