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., part of General ElectricLabelled 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 GE DEC Medical Systems with 10 510(k) clearances. The most recent is a 510(k) clearance dated Apr 11, 2000: SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM.
| Apr 11, 2000 | SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARMK000221 · OWB | 510(k) clearances |
| Dec 21, 1999 | UROVIEW 2800K993687 · OWB | 510(k) clearances |
| Aug 19, 1999 | MINI 6800 DIGITAL MOBILE C-ARMK992506 · OXO | 510(k) clearances |
| Feb 17, 1998 | INTERVENTIONAL MOBILE DIGITAL IMAGING SYSTEM (HEREIN CALLED IMDIS)K974355 · OWB | 510(k) clearances |
| Mar 11, 1997 | SERIES 7600 MOBILE DIGITAL C-ARMK970063 · OWB | 510(k) clearances |
| Dec 23, 1996 | SERIES 9600 MOBILE DIGITAL IMAGING SYSTEMK963952 · OWB | 510(k) clearances |
| Jun 5, 1995 | COMPACT 7600K950781 · JAA | 510(k) clearances |
| May 11, 1995 | SERIES 6600 DIGITAL MOBILE C-ARMK951765 · OXO | 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
