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 Labeltape Meditect with 26 510(k) clearances. The most recent is a 510(k) clearance dated Apr 25, 1995: LMI MEDICAL, ELECTRODE, ELECTROSURGICAL, DISPOSABLE DISPERSIVE ELECTRODE WITH CORD.
| Apr 25, 1995 | LMI MEDICAL, ELECTRODE, ELECTROSURGICAL, DISPOSABLE DISPERSIVE ELECTRODE WITH CORDK951328 · GEI | 510(k) clearances |
| Jan 14, 1992 | ELECTRODE USING PROMEON RG-60 SERIES GELK915333 · GXY | 510(k) clearances |
| Dec 18, 1991 | TRANS ELEC NERVE STIM/MUSCLE STIM ELEC W/POLY GELK914871 · GZJ | 510(k) clearances |
| Oct 4, 1991 | HEMAWIPE SYSTEM, THE CIVILIZED TEST, MODIFICATIONK912979 · KHE | 510(k) clearances |
| Sep 4, 1990 | ELECTRO BLUE ECG ELECTRODE-PEDIATRIC CLOTHK902738 · DRX | 510(k) clearances |
| Jul 19, 1990 | SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECTK902719 · GXY | 510(k) clearances |
| Mar 1, 1990 | SPEC T.E.N.S. PREWIRED REPOSITIONABLE TENS ELECT.K900656 · GXY | 510(k) clearances |
| Feb 12, 1990 | BABE-EASE NEONATAL CLOTH ECG ELECTRODEK896844 · 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
