Durtech System Corp.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 2
What Durtech System Corp. makes
Durtech System Corp. manufactures magnetic resonance imaging (MRI) compatible patient positioning and immobilization devices, including adjustable tables and restraint systems designed for use in diagnostic and therapeutic MRI procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Magbody Dt-600 Ref K053284
510(k) 510(k)
Frequently asked questions
How many devices does Durtech System Corp. have in the registry?
The registry currently lists 2 devices for Durtech System Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Durtech System Corp.'s devices?
Among its 2 most recently registered devices, Durtech System Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Durtech System Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Durtech System Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Durtech System Corp. in the registry?
The most recently registered devices listed for Durtech System Corp. include MAGBODY DT-1200, DT-1200T, DT-1200M, DT-1200PT, DT-1200PM and MAGBODY DT-600.