Thomson-Cgr Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Thomson-Cgr Medical Corp. makes
Thomson-Cgr Medical Corp. manufactures digital angiographic systems, including the DG 200/300 for vascular imaging, and MRI systems like the MAGNISCAN 5000 for soft tissue and organ visualization. Their portfolio also includes X-ray generators, such as the MPG-50, and stereotactic systems like STEREOTIX for precise surgical guidance.
The company’s devices are regulated under FDA pathways, including 510(k) clearances for Class II products and PMA submissions for Class I devices. These systems are listed in the FDA’s regulatory databases, and the manufacturer operates from the United States.
Catalogue
Dg 200/300 Digital Angiographic System Ref K852353
Regimes: 510(k) Registry: 510(k)Stereotix Ref K873618
Regimes: 510(k) Registry: 510(k)Mpg-50 X-Ray Generator Ref K873544
Regimes: 510(k) Registry: 510(k)Magniscan 5000 Mri System Ref P850043
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Thomson-Cgr Medical Corp. have in the registry?
The registry currently lists 4 devices for Thomson-Cgr Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thomson-Cgr Medical Corp.'s devices?
Among its 4 most recently registered devices, Thomson-Cgr Medical Corp. has devices listed in FDA 510(k) (3 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Thomson-Cgr Medical Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Thomson-Cgr Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thomson-Cgr Medical Corp. in the registry?
The most recently registered devices listed for Thomson-Cgr Medical Corp. include DG 200/300 DIGITAL ANGIOGRAPHIC SYSTEM, STEREOTIX, MPG-50 X-RAY GENERATOR and MAGNISCAN 5000 MRI SYSTEM.