# Kinetix

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1983–1984): 4 510(k) clearances
- Product codes: BYP (2), BZG (1), BWF (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
- K832401: Respirometer (Apr 30, 1984)
- K840459: Improved Mouthpiece (Feb 17, 1984)
- K833420: Kinetix Mouthpiece (Jan 10, 1984)
- K833012: Inspirometer (Nov 8, 1983)

Source page: https://510kreport.com/company/kinetix