Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012)
South KoreaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Portable X-ray System (Model: MINIX-V / MINIX-S) Ref K152859
Regimes: CE MDD 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) have in the registry?
The registry currently lists 1 device for Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012). Devices recorded under merged duplicate company entries are counted once.
Which registries list Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012)'s devices?
Among its 1 most recently registered device, Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) has devices listed in FDA 510(k) (1 device).
What risk classes do Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012)'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) in the registry?
The most recently registered devices listed for Digimed Co., Ltd. (Digimed Corporation Until 31/12/2012) include Portable X-ray System (Model: MINIX-V / MINIX-S).