# Rabar, Inc.

- Location (FDA's records): Rochester, NY
- FDA decisions: 3 (1982–1984): 3 510(k) clearances
- Product codes: GZJ (1), GFJ (1), GXW (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
- K844017: Microtens 7757 T.E.N.S. Stimulator (Nov 30, 1984)
- K842414: Echo Pulse Burst (Jul 27, 1984)
- K821736: Echo-Pulse KM555 (Dec 9, 1982)

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