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 14, 2026, FDA's public records list Siegen Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 1, 1987: SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU..
| Oct 1, 1987 | SIEGEN NEUROSCOPE SEEG FOR EVOKED RESPONSE STIMU.K871964 · GWF | 510(k) clearances |
| Oct 14, 1986 | NEUROSCOPE SEEGK861884 · GWO | 510(k) clearances |
| Sep 26, 1986 | SIEGEN HEADPHONESK862430 · GWJ | 510(k) clearances |
| Feb 14, 1985 | SIEGEN VISUAL STIMULATORK844616 · GWE | 510(k) clearances |
| Dec 11, 1984 | SIEGEN SURFACE ELECTRODESK844646 · GXY | 510(k) clearances |
| Nov 20, 1984 | SIEGEN NEUROSCOPEK843464 · GWF | 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
