# Fluidotherapy Corp.

- Location (FDA's records): Houston, TX
- FDA decisions: 3 (1983–1985): 3 510(k) clearances
- Product codes: HCC (1), IMI (1), IMJ (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
- K850573: Curamed 402 (May 17, 1985)
- K850640: Sonopuls 434 Ultrasound Therapy Equipment (May 14, 1985)
- K832122: Enraf NONIVS2 Channel Emg/Temp. Feed (Aug 12, 1983)

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