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 15, 2026, FDA's public records list Rigel Medical Electronics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 2, 1989: PATIENT MONITOR RIGEL MODEL MULTICARE 429.
| Feb 2, 1989 | PATIENT MONITOR RIGEL MODEL MULTICARE 429K884645 · DRT | 510(k) clearances |
| Jun 28, 1988 | RIGEL MODEL MULTICARE 409K875160 · DRT | 510(k) clearances |
| Apr 18, 1985 | NEONATAL MONITOR 309K850407 · DRT | 510(k) clearances |
| Mar 1, 1985 | ECG PATIENT MONITOR 301K850156 · DRT | 510(k) clearances |
| Mar 1, 1985 | ECG PATIENT MONITOR 302K850155 · DRT | 510(k) clearances |
| Dec 27, 1984 | ECG PATIENT MONITORK843376 · DRT | 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
