Selicor, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Selicor, Inc. makes
Selicor, Inc. manufactures the SELITHERM (Model C100), a thermal therapy device, and the SELICOR (Models A100 and D100), which appear to be related diagnostic or monitoring systems for medical use.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Selitherm, Model C100 Ref K030382
Regimes: 510(k) Registry: 510(k)Selicor, Models A100 & D100 Ref K020227
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Selicor, Inc. have in the registry?
The registry currently lists 2 devices for Selicor, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Selicor, Inc.'s devices?
Among its 2 most recently registered devices, Selicor, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Selicor, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Selicor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Selicor, Inc. in the registry?
The most recently registered devices listed for Selicor, Inc. include SELITHERM, MODEL C100 and SELICOR, MODELS A100 & D100.