# Katalyst, Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 3 (2017–2020): 3 510(k) clearances
- Product codes: NGX (3)
- 510(k) review time since 2016: median 153 days, against 108 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 4 (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
- Chattanooga Group, Inc.: 2 (https://510kreport.com/company/chattanooga-group)
- Fit-Pro Kft, Ltd.: 2 (https://510kreport.com/company/fit-pro-kft)
- Djo, LLC: 1 (https://510kreport.com/company/djo)

## Firms that cite its devices most
- Pepper Interactive, Inc.: 1 (https://510kreport.com/company/pepper-interactive)
- Fast Fit, LLC: 1 (https://510kreport.com/company/fast-fit)
- Miha Bodytec GmbH: 1 (https://510kreport.com/company/miha-bodytec)
- Vb Technologies AG: 1 (https://510kreport.com/company/vb-technologies)

## Its most-cited devices
- K190966: Katalyst Training System (2020), cited by 3
- K181199: Katalyst Mark 1 Muscle Stimulation System Model 2 (2018), cited by 1

## Recent decisions
- K190966: Katalyst Training System (Feb 3, 2020)
- K181199: Katalyst Mark 1 Muscle Stimulation System Model 2 (Sep 20, 2018)
- K171035: Katalyst Mark 1 Muscle Stimulation System (Sep 6, 2017)

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