# C. B. Dumont Company, Inc.

- Location (FDA's records): Newport, RI
- FDA decisions: 2 (1982–1986): 2 510(k) clearances
- Product codes: FPA (1), FMF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Henke-Sass, Wolf GmbH: 1 (https://510kreport.com/company/henke-sass-wolf)

## Its most-cited devices
- K821537: Henke Disposable Syringe (1982), cited by 1

## Recent decisions
- K854804: Multiple I.V. Sets (Feb 12, 1986)
- K821537: Henke Disposable Syringe (May 28, 1982)

Source page: https://510kreport.com/company/c-b-dumont