# Myo-Tronics, Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 6 (1991–1997): 6 510(k) clearances
- Product codes: KZM (3), NFQ (2), HCC (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Myotronics-Noromed, Inc.: 1 (https://510kreport.com/company/myotronics-noromed)

## Its most-cited devices
- K922270: Physiotech 4000 or Norodyn 8000 (1994), cited by 1

## Recent decisions
- K970116: Esg-1 Electrosonogram (Esg-1) (Apr 2, 1997)
- K944134: K6-1 Diagnostic System Version 3.1 (Dec 9, 1994)
- K922270: Physiotech 4000 or Norodyn 8000 (Sep 2, 1994)
- K922456: K6-I Diagnostic System (Jun 9, 1994)
- K921919: MS-100 Myo-Scanner or MS-100 Emg Scanner (Jan 7, 1993)
- K905449: Electrosonogram Esg-1 (Apr 26, 1991)

Source page: https://510kreport.com/company/myo-tronics