Daiwa Products, Inc.
Country not established
- Devices
- 1
What Daiwa Products, Inc. makes
Daiwa Products, Inc. manufactures the Daiwa Model 180, a Class II medical device designed for [specific use not provided in data]. The device is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The Daiwa Model 180 is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Daiwa Model 180 Ref K983616
510(k) 510(k)
Frequently asked questions
How many devices does Daiwa Products, Inc. have in the registry?
The registry currently lists 1 device for Daiwa Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Daiwa Products, Inc.'s devices?
Among its 1 most recently registered device, Daiwa Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Daiwa Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Daiwa Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Daiwa Products, Inc. in the registry?
The most recently registered devices listed for Daiwa Products, Inc. include DAIWA MODEL 180.