Dufco Electronics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
What Dufco Electronics, Inc. makes
Dufco Electronics, Inc. manufactures multimode interface systems and power module systems designed for compatibility with specific medical devices, including those from Everest, Jennings, and Meyra wheelchairs. These systems facilitate power and data connectivity between mobility aids and external power sources or control interfaces.
The company’s products are classified as Class II devices under FDA regulations and are subject to 510(k) clearance requirements. The portfolio is listed in the FDA’s 510(k) database, reflecting regulatory compliance for medical device distribution in the United States.
Catalogue
- 510(k) 510(k)
Unimode(Tm) Power Module System Ref K881462
510(k) 510(k)- 510(k) 510(k)
Multimode(Tm) Power Module System Ref K881463
510(k) 510(k)
Frequently asked questions
How many devices does Dufco Electronics, Inc. have in the registry?
The registry currently lists 4 devices for Dufco Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dufco Electronics, Inc.'s devices?
Among its 4 most recently registered devices, Dufco Electronics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Dufco Electronics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Dufco Electronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dufco Electronics, Inc. in the registry?
The most recently registered devices listed for Dufco Electronics, Inc. include MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNING, UNIMODE(TM) POWER MODULE SYSTEM, MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. and MULTIMODE(TM) POWER MODULE SYSTEM.