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 13, 2026, FDA's public records list Radkor, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Nov 13, 1989: RADKOR DXG-650R.
| Date | Record | Source |
|---|---|---|
| Nov 13, 1989 | RADKOR DXG-650RK895969 · IZO | 510(k) clearances |
| Apr 26, 1989 | RADKOR TS10-BK892196 · IXQ | 510(k) clearances |
| Apr 3, 1989 | RADKOR BS-10 AND BS-10TK891395 · IXY | 510(k) clearances |
| Oct 19, 1988 | RADKOR, RF-159K883885 · KXJ | 510(k) clearances |
| Oct 19, 1988 | RADKOR SFR-70K883864 · IYB | 510(k) clearances |
| Sep 8, 1988 | RADKOR SFC-21K881701 · IYB | 510(k) clearances |
| Sep 2, 1988 | RADKOR KOB-84K881700 · KXJ | 510(k) clearances |
| Sep 2, 1988 | RADKOR, XG-515K883081 · 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
