Sps, Inc.
Country not established
- Devices
- 1
What Sps, Inc. makes
Sps, Inc. manufactures the MAGNUM, a medical device designed for [specific clinical use not provided in data]. This product falls under the category of [device type not specified in data], addressing [unclear functional purpose from given data].
The MAGNUM is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company operates within the United States, adhering to domestic regulatory requirements for medical devices.
Catalogue
Magnum Ref K932902
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sps, Inc. have in the registry?
The registry currently lists 1 device for Sps, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sps, Inc.'s devices?
Among its 1 most recently registered device, Sps, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sps, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sps, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sps, Inc. in the registry?
The most recently registered devices listed for Sps, Inc. include MAGNUM.