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 14, 2026, FDA's public records list Myo-Tronics with 6 510(k) clearances. The most recent is a 510(k) clearance dated Apr 2, 1997: ESG-1 ELECTROSONOGRAM (ESG-1).
| Apr 2, 1997 | ESG-1 ELECTROSONOGRAM (ESG-1)K970116 · NFQ | 510(k) clearances |
| Dec 9, 1994 | K6-1 DIAGNOSTIC SYSTEM VERSION 3.1K944134 · KZM | 510(k) clearances |
| Sep 2, 1994 | PHYSIOTECH 4000 OR NORODYN 8000K922270 · HCC | 510(k) clearances |
| Jun 9, 1994 | K6-I DIAGNOSTIC SYSTEMK922456 · KZM | 510(k) clearances |
| Jan 7, 1993 | MS-100 MYO-SCANNER OR MS-100 EMG SCANNERK921919 · KZM | 510(k) clearances |
| Apr 26, 1991 | ELECTROSONOGRAM ESG-1K905449 · NFQ | 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
