Logos Medical Co., Ltd.
JapanFDA applicant, unverified
- Devices
- 1
What Logos Medical Co., Ltd. makes
Logos Medical Co., Ltd. manufactures electrocardiogram (ECG) devices, specifically a single-channel direct-writing electrocardiograph for recording heart activity.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Logos Medical Co., Ltd. have in the registry?
The registry currently lists 1 device for Logos Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Logos Medical Co., Ltd.'s devices?
Among its 1 most recently registered device, Logos Medical Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Logos Medical Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Logos Medical Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Logos Medical Co., Ltd. in the registry?
The most recently registered devices listed for Logos Medical Co., Ltd. include LOGOS8821 1-CHANNEL DIRECT-WRITING ELECTROCARDIOGR.