# Hudson Oxygen Therapy Sales Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 33 (1976–1990): 33 510(k) clearances
- Product codes: CAF (4), CAW (3), CBP (2), CAH (2), BTM (2), BYI (2), BZO (2), CAP (2), FLK (1), BYE (1), CAT (1), CBH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 11 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- A Plus Medical: 2 (https://510kreport.com/company/a-plus-medical)
- Promedic, Inc.: 2 (https://510kreport.com/company/promedic)
- Fisher & Paykel Healthcare, Ltd.: 1 (https://510kreport.com/company/fisher-paykel-healthcare)
- Hsiner Co., Ltd.: 1 (https://510kreport.com/company/hsiner)
- Mergenet Medical: 1 (https://510kreport.com/company/mergenet-medical)
- Galemed Corp.: 1 (https://510kreport.com/company/galemed)
- Steve Islava: 1 (https://510kreport.com/company/steve-islava)
- Airways Ltd., Inc.: 1 (https://510kreport.com/company/airways)

## Its most-cited devices
- K902062: Peep Valve (1990), cited by 4
- K871157: C.P.a.P. Nasal Cannula (1987), cited by 3
- K760489: Nebulizer, Handheld (T UP-Draft) (1976), cited by 1
- K770771: Aerosol Effusion System #1740 (1977), cited by 1
- K781831: Spirometer, Incentive Catalog # 1750 (1978), cited by 1
- K895589: Manual Resuscitator (1990), cited by 1

## Recent decisions
- K902062: Peep Valve (Sep 4, 1990)
- K900783: Mdi Adaptor (Jul 18, 1990)
- K900470: IN-the Nebulizer (May 18, 1990)
- K895589: Manual Resuscitator (Mar 30, 1990)
- K896136: Infant C.P.a.P. Monitor (Jan 9, 1990)
- K895747: Ventilarm II Portable Airway Pressure Monitor (Oct 27, 1989)
- K895231: Catalog NO. 1755 1S0-Neb, a Filtered Nebulizer (Oct 27, 1989)
- K890035: Bacteria Filter (May 5, 1989)

Source page: https://510kreport.com/company/hudson-oxygen-therapy-sales