# Myo/Kinetic Systems, Inc.

- Location (FDA's records): Menomonee Falls, WI
- FDA decisions: 8 (1992–1995): 8 510(k) clearances
- Product codes: IPF (3), KPI (1), HIR (1), EXY (1), FEN (1), GZJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K945937: TE-800 Pelvic Floor Exerciser (Jul 14, 1995)
- K945292: TS-700P Control XP Electrical Stimulator (Apr 12, 1995)
- K944972: Uro-Gram Cystomrtrogram with Uroflowmetry (Mar 8, 1995)
- K936041: Urogram Cystometrogram (Apr 18, 1994)
- K932611: Neuromuscular Stimulator (Jan 31, 1994)
- K932764: Therapeutic Stimulator 300(TS-300) & 300P (TS-300P) (Oct 1, 1993)
- K932399: Therapeutic Stim 200 (TS-200)/200P (TS-200P) (Aug 11, 1993)
- K914904: Therapeutic Stimulator 2100 (TS-2100) (Apr 28, 1992)

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