# Prothia USA, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 5 (1982–1983): 5 510(k) clearances
- Product codes: BXN (2), GZX (1), GFD (1), GCJ (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
- K831071: Universal Instru. Set for Neurovascular (Jun 8, 1983)
- K830993: Ampligreffe (May 3, 1983)
- K823581: ELPHA 500 (Mar 24, 1983)
- K830058: Myograph 2000 (Mar 7, 1983)
- K823583: Myotest Nerve Stimulator (Dec 30, 1982)

Source page: https://510kreport.com/company/prothia-usa