Afx, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Afx Microwave Generator, Flex Ablation Wand, Lynx Ablation Wand, Model Series 1000, P/N 102006, P/N 102007 Ref K003978
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Afx, Inc. have in the registry?
The registry currently lists 2 devices for Afx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Afx, Inc.'s devices?
Among its 2 most recently registered devices, Afx, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Afx, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Afx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Afx, Inc. in the registry?
The most recently registered devices listed for Afx, Inc. include AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007 and FLEX 10 ACCESSORY FOR THE AFX MICROWAVE ABLATION SYSTEM.