Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in NetherlandsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of ElektaLabelled 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 Nucletron-Oldelft Corp. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Aug 13, 1996: MICROSELECTRON-HDR VERSION 2.
| Aug 13, 1996 | MICROSELECTRON-HDR VERSION 2K953946 · JAQ | 510(k) clearances |
| Sep 8, 1995 | N 800 HFK953831 · IZO | 510(k) clearances |
| Nov 19, 1993 | MICROSELECTRON - HDR FOR MOBILE ENVIRONMENTK925956 · JAQ | 510(k) clearances |
| Mar 31, 1993 | MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILMK926407 · KXJ | 510(k) clearances |
| Nov 27, 1992 | PLATO RADIATION THERAPY PLANNING SYSTEMK921991 · IYE | 510(k) clearances |
| Sep 25, 1992 | PLATO BRACHYTHERAPHY TREATMENT PLANNING SYSTEMK915622 · JAQ | 510(k) clearances |
| Jun 13, 1991 | NUCLETRON PLANNING SYSTEMK911612 · IYE | 510(k) clearances |
| Oct 12, 1990 | PULSED SELECTRONK902533 · JAQ | 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
