Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 13, 2026, FDA's public records list General X-Ray, Inc. with 14 510(k) clearances. The most recent is a 510(k) clearance dated May 28, 1980: ATLAS-S X-RAY SYSTEM W/KETROMAT GEN..
| May 28, 1980 | ATLAS-S X-RAY SYSTEM W/KETROMAT GEN.K800998 · | 510(k) clearances |
| Mar 28, 1979 | X-RAY UNITS, GX-101, UCIS-510 AND GX-111K790451 · IZL | 510(k) clearances |
| Mar 26, 1979 | MOBILE X-RAY UNITK790511 · IZL | 510(k) clearances |
| Mar 26, 1979 | PORTABLE X-RAY UNITK790443 · IZL | 510(k) clearances |
| Mar 26, 1979 | PORTABLE X-RAY UNIT, MATRIX S GX-101K790393 · IZL | 510(k) clearances |
| Mar 26, 1979 | PORTABLE X-RAY UNITK790512 · IZL | 510(k) clearances |
| Mar 26, 1979 | 510 CARBINETTE X-RAY UNITK790392 · IZL | 510(k) clearances |
| Dec 4, 1978 | MOBILE X-RAY UNITK781976 · IZL | 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
