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 D&R X-Ray Products, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 1, 1986: CEILSTAND, MULTISTAND R & S AND THE BUCKYSTAND.
| Aug 1, 1986 | CEILSTAND, MULTISTAND R & S AND THE BUCKYSTANDK862734 · IYB | 510(k) clearances |
| Jul 25, 1986 | COLLIMATOR MODEL A280BLMD & MODEL A280BLMPK861941 · IZX | 510(k) clearances |
| Jul 25, 1986 | COLLIMATOR MODEL A280BLE & MODEL A280-BLMK861942 · IZW | 510(k) clearances |
| May 29, 1986 | RADIOGRAPHIC TABLES MODELS A71OS-T,A71OT-T,A71OB-TK861940 · IZZ | 510(k) clearances |
| Apr 10, 1985 | TILTING TABLE RADIOGRAPHIC A9006 TOMOJUPITERK850948 · IXR | 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
