Cyberlogic, Inc.
Country not established FDA FEI 3005944888
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Cyberlogic, Inc. makes
Cyberlogic, Inc. manufactures the UltraScan 650, a medical imaging device designed for diagnostic ultrasound applications, including internal organ visualization and procedural guidance.
The UltraScan 650 is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
UltraScan 650 Ref K161919
510(k) 510(k)
Company details
- FDA FEI number
- 3005944888
- Address
- 112 Willow Street, Brooklyn, NY, 11201
Frequently asked questions
How many devices does Cyberlogic, Inc. have in the registry?
The registry currently lists 1 device for Cyberlogic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cyberlogic, Inc.'s devices?
Among its 1 most recently registered device, Cyberlogic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cyberlogic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cyberlogic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cyberlogic, Inc. in the registry?
The most recently registered devices listed for Cyberlogic, Inc. include UltraScan 650.