Amertek Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Amertek Medical, Inc. makes
Amertek Medical, Inc. makes medical devices such as the AMERITEK SURE-POINT TRACKER SYSTEM, AMERITEK SURE-POINT HDR NEEDLE TEMPLATE, and AMERITEK BRACHYTHERAPY TEMPLATE, which are types of tracking and brachytherapy systems and templates.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Ameritek Sure-Point Tracker System Ref K030518
Regimes: 510(k) Registry: 510(k)Ameritek Sure-Point Hdr Needle Template Ref K031273
Regimes: 510(k) Registry: 510(k)Ameritek Brachytherapy Template Ref K011581
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Amertek Medical, Inc. have in the registry?
The registry currently lists 3 devices for Amertek Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amertek Medical, Inc.'s devices?
Among its 3 most recently registered devices, Amertek Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Amertek Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Amertek Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amertek Medical, Inc. in the registry?
The most recently registered devices listed for Amertek Medical, Inc. include AMERITEK SURE-POINT TRACKER SYSTEM, AMERITEK SURE-POINT HDR NEEDLE TEMPLATE and AMERITEK BRACHYTHERAPY TEMPLATE.