Dongjin Medical Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What Dongjin Medical Co., Ltd. makes
Dongjin Medical Co., Ltd. manufactures the I-SCOPE 200, a flexible endoscope designed for diagnostic and therapeutic procedures in internal body cavities.
The I-SCOPE 200 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
I-Scope 200 Ref K062364
510(k) 510(k)
Frequently asked questions
How many devices does Dongjin Medical Co., Ltd. have in the registry?
The registry currently lists 1 device for Dongjin Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dongjin Medical Co., Ltd.'s devices?
Among its 1 most recently registered device, Dongjin Medical Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Dongjin Medical Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dongjin Medical Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dongjin Medical Co., Ltd. in the registry?
The most recently registered devices listed for Dongjin Medical Co., Ltd. include I-SCOPE 200.