Magna Advanced Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
What Magna Advanced Technologies, Inc. makes
Magna Advanced Technologies, Inc. makes electrosurgical units and related devices, including models such as the MAGNATEK C-300, MAGNATEK 30, MTEK-1400, MAGNATEK 40, MTEK-1000, MAGNATEK ELECTROSURGICAL UNITS MODELS ESU-10 and ESU-15, and MAGNATEK80.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Magnatek C-300 Ref K981310
Regimes: 510(k) Registry: 510(k)Magnatek 30 Ref K991819
Regimes: 510(k) Registry: 510(k)Mtek-1400 Ref K982846
Regimes: 510(k) Registry: 510(k)Magnatek 40 Ref K982907
Regimes: 510(k) Registry: 510(k)Mtek-1000 Ref K982405
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
MAGNATEK80 Ref K983114
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Magna Advanced Technologies, Inc. have in the registry?
The registry currently lists 7 devices for Magna Advanced Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magna Advanced Technologies, Inc.'s devices?
Among its 7 most recently registered devices, Magna Advanced Technologies, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Magna Advanced Technologies, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Magna Advanced Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Magna Advanced Technologies, Inc. in the registry?
The most recently registered devices listed for Magna Advanced Technologies, Inc. include MAGNATEK C-300, MAGNATEK 30, MTEK-1400 and MAGNATEK 40.