Kyong-Buk Trading Corp.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What Kyong-Buk Trading Corp. makes
Kyong-Buk Trading Corp. manufactures the KBTC, a medical device designed for specific diagnostic or procedural use within Class I regulatory categorization. This product is intended for applications requiring low-risk intervention, such as basic monitoring or non-invasive procedures.
The KBTC is regulated under the FDA’s 510(k) pathway as a Class I device, indicating it meets minimal risk standards for medical devices. The company is based in the United States, where its product is listed for compliance with U.S. regulatory requirements.
Catalogue
Kbtc Ref K950720
510(k) 510(k)
Frequently asked questions
How many devices does Kyong-Buk Trading Corp. have in the registry?
The registry currently lists 1 device for Kyong-Buk Trading Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kyong-Buk Trading Corp.'s devices?
Among its 1 most recently registered device, Kyong-Buk Trading Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Kyong-Buk Trading Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kyong-Buk Trading Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kyong-Buk Trading Corp. in the registry?
The most recently registered devices listed for Kyong-Buk Trading Corp. include KBTC.