Marshall Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Marshall Electronics, Inc. makes
Marshall Electronics, Inc. manufactures emergency medical trauma kits, manual breast pumps (Kaneson/Comfort Plus), and electronic black bag resuscitation systems designed for pre-hospital and field use.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Auto Trauma Kit Ref K790411
Regimes: 510(k) Registry: 510(k)Kaneson/Comfort Plus Manual Breast Pump Ref K813247
Regimes: 510(k) Registry: 510(k)Black Bag, Electronic Ref K780023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Marshall Electronics, Inc. have in the registry?
The registry currently lists 3 devices for Marshall Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Marshall Electronics, Inc.'s devices?
Among its 3 most recently registered devices, Marshall Electronics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Marshall Electronics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Marshall Electronics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Marshall Electronics, Inc. in the registry?
The most recently registered devices listed for Marshall Electronics, Inc. include AUTO TRAUMA KIT, KANESON/COMFORT PLUS MANUAL BREAST PUMP and BLACK BAG, ELECTRONIC.