# Bomed Medical Mfr., Ltd.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 8 (1981–1986): 8 510(k) clearances
- Product codes: DSB (4), IPF (1), DRX (1), GZJ (1), DXG (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
- K853706: Bomed-CDM (Apr 14, 1986)
- K853705: Bomed-Eea (Jan 13, 1986)
- K831421: Bomed Biocon (Sep 12, 1983)
- K831422: Bioflow (Sep 12, 1983)
- K830792: Pulsette 110 Transcutaneous Elec-Nerve (Mar 29, 1983)
- K813020: Bomed-Nccom (Dec 14, 1981)
- K811999: BO Med Bia (Aug 31, 1981)
- K810064: Pulsarii, High Volt. Galvanic Musc. Stim (Jan 26, 1981)

Source page: https://510kreport.com/company/bomed-medical-mfr