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 15, 2026, FDA's public records list Bay X-Ray with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 21, 1988: HIMOBILIX 2N.
| Oct 21, 1988 | HIMOBILIX 2NK883161 · JAA | 510(k) clearances |
| Sep 8, 1988 | CATAPULT BUCKY (KATAPULT BLENDA)K883160 · KPR | 510(k) clearances |
| Sep 6, 1988 | SELDIX 325 TWO PULSE GENERATOR/CONTROLK883154 · IZO | 510(k) clearances |
| Sep 6, 1988 | TELESTATIX X-RAY TABLEK883162 · IXR | 510(k) clearances |
| Sep 6, 1988 | UNDISTAT WITH EXPLORATOR 35 (UCS 35E)K883153 · IXR | 510(k) clearances |
| Sep 6, 1988 | RASTIX X-RAY TABLEK883155 · KXJ | 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
