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 Jason Marketing Co. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 30, 1992: ELECTROTRACE, MODIFICATION.
| Oct 30, 1992 | ELECTROTRACE, MODIFICATIONK924133 · DRX | 510(k) clearances |
| Nov 5, 1990 | ELECTROTRACE DISPOSABLE AG/AGCL EKG MON. ELEC.K903555 · DRX | 510(k) clearances |
| Jan 18, 1990 | ELECTROTRACE DISPOSABLE AG/AGCL EKG MONITOR ELEC.K896569 · DRX | 510(k) clearances |
| Sep 13, 1989 | ELECTROTRACE DISP. RESTING EKG ELECTRODESK894679 · DRX | 510(k) clearances |
| Jun 5, 1987 | ELECTROTRACE DISP REST EKG ELECTRODE, CAT. ET1200K871626 · DRX | 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
