# H&A Mui Enterprises, Inc.

- Location (FDA's records): Mississauga, CA
- FDA decisions: 2 (2020–2023): 2 510(k) clearances
- Product codes: FED (1), EOB (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- United States Endoscopy Group, Inc.: 1 (https://510kreport.com/company/united-states-endoscopy-group)
- Schoelly Fiberoptic GmbH: 1 (https://510kreport.com/company/schoelly-fiberoptic)

## Recent decisions
- K222587: PatCom Distal Chip Endoscope (Jul 28, 2023)
- K192691: PatCom Single-Use Introducer (Feb 21, 2020)

Source page: https://510kreport.com/company/h-a-mui-enterprises