# Motion Lab Systems, Inc.

- Location (FDA's records): Baton Rouge, LA
- FDA decisions: 2 (1998–2000): 2 510(k) clearances
- Product codes: IKN (2)
- Predicates its devices cite: 1 (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 whose devices it cites most
- B & L Engineering: 1 (https://510kreport.com/company/b-l-engineering)

## Firms that cite its devices most
- Uroval: 1 (https://510kreport.com/company/uroval)

## Its most-cited devices
- K000220: MA-300 Electromyography System (2000), cited by 1

## Recent decisions
- K000220: MA-300 Electromyography System (Feb 24, 2000)
- K974385: MLS Electromyographic Preamplifier (Feb 19, 1998)

Source page: https://510kreport.com/company/motion-lab-systems