Yamasu Co., Ltd.
JapanFDA 510(k) applicant, unverified
- Devices
- 2
What Yamasu Co., Ltd. makes
Yamasu Co., Ltd. manufactures aneroid-based blood pressure measurement devices, including a home blood pressure kit and a doctor-type sphygmomanometer designed for clinical use.
These devices are regulated under FDA Class II and Class III classifications, with authorisation records maintained in the 510(k) premarket notification database. The company is based in the United States.
Catalogue
Home Blood Pressure Kit, Aneroid Ref K884420
510(k) 510(k)Aneroid Sphygmomanometer, Doctor Type Ref K901506
510(k) 510(k)
Frequently asked questions
How many devices does Yamasu Co., Ltd. have in the registry?
The registry currently lists 2 devices for Yamasu Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yamasu Co., Ltd.'s devices?
Among its 2 most recently registered devices, Yamasu Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Yamasu Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Yamasu Co., Ltd.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Yamasu Co., Ltd. in the registry?
The most recently registered devices listed for Yamasu Co., Ltd. include HOME BLOOD PRESSURE KIT, ANEROID and ANEROID SPHYGMOMANOMETER, DOCTOR TYPE.