Trismed Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What Trismed Co., Ltd. makes
Trismed Co., Ltd. manufactures portable electrocardiogram (ECG) devices, including the CARDIPIA400H and CARDIPIA800H models, designed for cardiac monitoring and diagnostic purposes.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
CARDIPIA ECG / Model: CARDIPIA400H, CARDIPIA800H Ref K230834
510(k) 510(k)
Frequently asked questions
How many devices does Trismed Co., Ltd. have in the registry?
The registry currently lists 1 device for Trismed Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trismed Co., Ltd.'s devices?
Among its 1 most recently registered device, Trismed Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Trismed Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Trismed Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trismed Co., Ltd. in the registry?
The most recently registered devices listed for Trismed Co., Ltd. include CARDIPIA ECG / Model: CARDIPIA400H, CARDIPIA800H.