Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 QMed, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Dec 3, 1998: MONITOR ONE NDX.
| Date | Record | Source |
|---|---|---|
| Dec 3, 1998 | MONITOR ONE NDXK972991 · DPS | 510(k) clearances |
| Dec 3, 1993 | PROFILOMATK932109 · DXN | 510(k) clearances |
| Oct 21, 1992 | INTERP-1000K921476 · LOS | 510(k) clearances |
| Apr 30, 1990 | QEKG ELECTROCARDIOGRAPHK897121 · DPS | 510(k) clearances |
| Sep 30, 1987 | A.R.M. (ASPEN RETURN MONITOR)K873591 · GEI | 510(k) clearances |
| Sep 26, 1986 | QMED SELF ADHERING ELECTRODEK862377 · GXY | 510(k) clearances |
| Aug 29, 1986 | BICORD BY QMEDK863091 · HAM | 510(k) clearances |
| May 20, 1986 | QMED SYSTEM 2150K861437 · DXG | 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
