Fathom Ent., Inc.
Country not established
- Devices
- 1
What Fathom Ent., Inc. makes
Fathom Ent., Inc. manufactures the FATHOM CMP-1000, a medical device designed for cardiac mapping and electroanatomical visualization, used in electrophysiology procedures to guide ablation therapies.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Fathom Cmp-1000 Ref K930051
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fathom Ent., Inc. have in the registry?
The registry currently lists 1 device for Fathom Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fathom Ent., Inc.'s devices?
Among its 1 most recently registered device, Fathom Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fathom Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fathom Ent., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fathom Ent., Inc. in the registry?
The most recently registered devices listed for Fathom Ent., Inc. include FATHOM CMP-1000.