Barzell-Whitmore Maroon Bells, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Barzell-Whitmore Maroon Bells, Inc. makes
Barzell-Whitmore Maroon Bells, Inc. manufactures accessories and equipment for brachytherapy procedures, including stepping units, needle guides, and support templates for precise radiation delivery. Their portfolio also includes a colo-rectal mover designed to assist in positioning during medical imaging or treatment.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are intended for use in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barzell-Whitmore Maroon Bells, Inc. have in the registry?
The registry currently lists 2 devices for Barzell-Whitmore Maroon Bells, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barzell-Whitmore Maroon Bells, Inc.'s devices?
Among its 2 most recently registered devices, Barzell-Whitmore Maroon Bells, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Barzell-Whitmore Maroon Bells, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Barzell-Whitmore Maroon Bells, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barzell-Whitmore Maroon Bells, Inc. in the registry?
The most recently registered devices listed for Barzell-Whitmore Maroon Bells, Inc. include BRACHYSTEPPER STEPPING UNIT, BRACHYSTEPPER NEEDLE GUIDE TEMPLATE, BRACHYSTAND SUPPORT AND MANUAL ADJUSTMENT ACCESSORY and BARZELL-WHITMORE MAROON BELLS, INC. COLO-RECTAL MOVER, MODEL 3900.