C. B. Dumont Company, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What C. B. Dumont Company, Inc. makes
C. B. Dumont Company, Inc. manufactures disposable intravenous (I.V.) sets and Henke disposable syringes, designed for single-use medical procedures.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Multiple I.V. Sets Ref K854804
510(k) 510(k)Henke Disposable Syringe Ref K821537
510(k) 510(k)
Frequently asked questions
How many devices does C. B. Dumont Company, Inc. have in the registry?
The registry currently lists 2 devices for C. B. Dumont Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C. B. Dumont Company, Inc.'s devices?
Among its 2 most recently registered devices, C. B. Dumont Company, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do C. B. Dumont Company, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for C. B. Dumont Company, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C. B. Dumont Company, Inc. in the registry?
The most recently registered devices listed for C. B. Dumont Company, Inc. include MULTIPLE I.V. SETS and HENKE DISPOSABLE SYRINGE.