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 14, 2026, FDA's public records list Continental X-Ray Corp. with 27 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 1997: CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002.
| Sep 11, 1997 | CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002K972442 · JAA | 510(k) clearances |
| Jul 25, 1996 | ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300K962140 · JAA | 510(k) clearances |
| Jun 27, 1996 | CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105K961690 · JAA | 510(k) clearances |
| Dec 21, 1995 | ARC SERIESK954581 · IZI | 510(k) clearances |
| Mar 31, 1995 | LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270K950571 · IZF | 510(k) clearances |
| Aug 17, 1994 | LINEAR TOMOGRAPHIC SYSTEM: PMT 6000K942175 · IZF | 510(k) clearances |
| Jun 7, 1994 | MODEL TM EP HIGH VOLTAGE GENERATORK942100 · IZO | 510(k) clearances |
| May 26, 1994 | MOLYBDENUM/RHODIUM FILTERSK934686 · IZO | 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
