Culligan Soft Water Service Co.
United Statesfrom the FDA registration address FDA establishment FEI 3007153372
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3007153372
- Address
- 6030 CULLIGAN WAY, Minnetonka, MN, 55345
Frequently asked questions
How many devices does CULLIGAN SOFT WATER SERVICE CO. have in the registry?
The registry currently lists 1 device for CULLIGAN SOFT WATER SERVICE CO.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CULLIGAN SOFT WATER SERVICE CO.'s devices?
Among its 1 most recently registered device, CULLIGAN SOFT WATER SERVICE CO. has devices listed in FDA 510(k) (1 device).
What risk classes do CULLIGAN SOFT WATER SERVICE CO.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for CULLIGAN SOFT WATER SERVICE CO.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CULLIGAN SOFT WATER SERVICE CO. in the registry?
The most recently registered devices listed for CULLIGAN SOFT WATER SERVICE CO. include DEIONIZER AND CARBON EXCHANGE SERVICE FOR HEMODIALYSIS.