GE Med. Systems Ultrasound & Prim. Care Diag., LLC
United StatesFDA applicant, unverified
- Devices
- 2
What GE Med. Systems Ultrasound & Prim. Care Diag., LLC makes
The company manufactures diagnostic ultrasound systems, including the GE Logiq 9 series (models 2404587 and 2375600-X), designed for medical imaging in primary care and specialty diagnostics.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Ge Logiq 9 Ultrasound BT03/Iq, Model 2375600-X Ref K032656
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ge Med. Systems Ultrasound & Prim. Care Diag., Llc have in the registry?
The registry currently lists 2 devices for Ge Med. Systems Ultrasound & Prim. Care Diag., Llc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Med. Systems Ultrasound & Prim. Care Diag., Llc's devices?
Among its 2 most recently registered devices, Ge Med. Systems Ultrasound & Prim. Care Diag., Llc has devices listed in FDA 510(k) (2 devices).
What risk classes do Ge Med. Systems Ultrasound & Prim. Care Diag., Llc's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ge Med. Systems Ultrasound & Prim. Care Diag., Llc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Med. Systems Ultrasound & Prim. Care Diag., Llc in the registry?
The most recently registered devices listed for Ge Med. Systems Ultrasound & Prim. Care Diag., Llc include GE LOGIQ 9 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL 2404587 and GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X.