# Myo-Tronics Research, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1977–1984): 8 510(k) clearances
- Product codes: NUW (3), KZM (2), EFH (1), IPF (1), DCN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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.: 3 (https://510kreport.com/company/myotronics-noromed)

## Its most-cited devices
- K842223: J4 Myo-Monitor (1984), cited by 2
- K842224: BNS 40 (1984), cited by 1

## Recent decisions
- K842223: J4 Myo-Monitor (Nov 19, 1984)
- K842224: BNS 40 (Nov 19, 1984)
- K833132: Mucosal Adjustment Paste Liquid Spray (Feb 10, 1984)
- K831364: Testcorp RA (May 27, 1983)
- K830034: Model EM-2 Bioelectric Processor (Feb 9, 1983)
- K813533: Electric Muscle Stimulator (Mar 5, 1982)
- K810528: Model EM-IR (Mar 31, 1981)
- K770252: Monitor, Myo, Model J3 (Feb 18, 1977)

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