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 15, 2026, FDA's public records list Myotronics-Noromed with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 29, 2011: EMG SYSTEM.
| Sep 29, 2011 | EMG SYSTEMK111687 · HCC | 510(k) clearances |
| Jul 20, 2004 | MYO-TRODE SG DISPOSABLE ELECTRODEK040400 · NUW | 510(k) clearances |
| Jul 24, 2003 | MODEL J-5 MVO-MONITORK031998 · NUW | 510(k) clearances |
| Nov 13, 2001 | MODEL MES-9000/EMG SYSTEMK013399 · HCC | 510(k) clearances |
| Nov 6, 2000 | MODEL K7 EVALUATION DEVICEK003287 · KZM | 510(k) clearances |
| Sep 10, 1999 | MODIFICATION TO K6-I DIAGNOSTIC SYSTEM, MODEL K6-IK992694 · KZM | 510(k) clearances |
| Aug 13, 1999 | NORODYN 8000 SEMG SYSTEM, ND-8000K992439 · HCC | 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
