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-Western Electronics, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 27, 1981: BIO-STIMULATOR, MODEL 400.
| Nov 27, 1981 | BIO-STIMULATOR, MODEL 400K813100 · GZJ | 510(k) clearances |
| Mar 30, 1981 | LITRONIC STIMULATORK810225 · IPF | 510(k) clearances |
| Oct 23, 1980 | VIEW-LITE, MODEL-DLK802216 · IXC | 510(k) clearances |
| Oct 23, 1980 | VIEW-LITE, MODEL-SK802215 · IXC | 510(k) clearances |
| Oct 23, 1980 | VIEW-LITE, MODEL-SLK802217 · IXC | 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
