Shockim Enterprises, Ltd.
Country not established
- Devices
- 2
What Shockim Enterprises, Ltd. makes
Shockim Enterprises, Ltd. manufactures external defibrillators, specifically the RHYTHM TOUCH Q 2-WAY, designed for automated or semi-automated cardiac rhythm analysis and shock delivery in emergency cardiac arrest scenarios.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Rhythm Touch Q 2-Way Ref K063743
Regimes: 510(k) Registry: 510(k)Rhythm Touch Q 2-Way Ref K032178
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Shockim Enterprises, Ltd. have in the registry?
The registry currently lists 2 devices for Shockim Enterprises, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shockim Enterprises, Ltd.'s devices?
Among its 2 most recently registered devices, Shockim Enterprises, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Shockim Enterprises, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Shockim Enterprises, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Shockim Enterprises, Ltd. in the registry?
The most recently registered devices listed for Shockim Enterprises, Ltd. include RHYTHM TOUCH Q 2-WAY.