FDA applicant
Hudson Oxygen Therapy Sales Co.
FDA records 33 decisions for Hudson Oxygen Therapy Sales Co. (Mchenry, IL) from 1976 to 1990: 33 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and CAW (Generator, Oxygen, Portable). 5 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Hudson Oxygen Therapy Sales Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hudson Oxygen Therapy Sales Co. since 2007.
Recalls per year
5in 2007
Class I Class II/III not classified
Planning a device like Hudson Oxygen Therapy Sales Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Hudson”
FDA records each applicant name separately; these may or may not be the same firm.