Seymour W. Meyer
Country not established
- Devices
- 1
What Seymour W. Meyer makes
Seymour W. Meyer manufactures the Meyer Foreign Body Locator, a medical device used to detect and locate foreign objects within the body.
The device is classified as Class II and is listed in the FDA 510(k) registry. Seymour W. Meyer is based in the United States. This record supports the regulatory information for the listed device.
Catalogue
Meyer Foreign Body Locator Ref K920470
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seymour W. Meyer have in the registry?
The registry currently lists 1 device for Seymour W. Meyer. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seymour W. Meyer's devices?
Among its 1 most recently registered device, Seymour W. Meyer has devices listed in FDA 510(k) (1 device).
What risk classes do Seymour W. Meyer's devices fall under?
Among its 1 most recently registered device, the classes recorded for Seymour W. Meyer's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seymour W. Meyer in the registry?
The most recently registered devices listed for Seymour W. Meyer include MEYER FOREIGN BODY LOCATOR.