# Mui Scientific

- Location (FDA's records): Mississauga, CA
- FDA decisions: 5 (1983–2026): 5 510(k) clearances
- Names in FDA's records: Mui Scientific (4); Mui Scientific, Inc. (1)
- Product codes: FFX (5)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (1 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
- G & J Electronics, Inc.: 2 (https://510kreport.com/company/g-j-electronics)

## Firms that cite its devices most
- Pentax Precision Instrument Corp.: 1 (https://510kreport.com/company/pentax-precision-instrument)
- Medspira, LLC: 1 (https://510kreport.com/company/medspira)
- Neuraxis: 1 (https://510kreport.com/company/neuraxis)

## Its most-cited devices
- K823701: Motility Catheters (1983), cited by 3
- K160287: Rapid Barostat Bag (RBB) Pump and Catheter (2017), cited by 1

## Recent decisions
- K262621: Rapid Barostat Bag (RBB) Pump and Catheter System (Sep 30, 2026)
- K160287: Rapid Barostat Bag (RBB) Pump and Catheter (Mar 14, 2017)
- K122294: Pressurized Infusion Pump (Nov 1, 2012)
- K120524: Sphincter of Oddi Manometric (Som) System (Jun 21, 2012)
- K823701: Motility Catheters (Feb 15, 1983)

Source page: https://510kreport.com/company/mui-scientific