DistributorLabelled 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 Neuro Supplies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 18, 1999: CUTANEOUS (GROUND) ELECTRODE.
| Aug 18, 1999 | CUTANEOUS (GROUND) ELECTRODEK991770 · GXY | 510(k) clearances |
| Aug 18, 1999 | DIGITAL RING ELECTRDEK991771 · GXY | 510(k) clearances |
| Aug 18, 1999 | CUTANEOUS (BAR) ELECTRODEK991769 · GXY | 510(k) clearances |
| Aug 18, 1999 | CUTANEOUS (DISC) ELECTRODEK991772 · GXY | 510(k) clearances |
| Jan 31, 1995 | NEUROLINK EEG/EP/EMG SURFACE ELECTRODESK942921 · GXY | 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
