# Marshall Electronics, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 3 (1978–1981): 3 510(k) clearances
- Product codes: HGY (1), KME (1), LDE (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
- K813247: Kaneson/Comfort Plus Manual Breast Pump (Dec 3, 1981)
- K790411: Auto Trauma Kit (Jun 1, 1979)
- K780023: Black Bag, Electronic (Feb 21, 1978)

Source page: https://510kreport.com/company/marshall-electronics