Bertone & Assoc.
Country not established
- Devices
- 1
What Bertone & Assoc. makes
Bertone & Assoc. manufactures the TIGER PULSE, a medical device designed for external cardiac defibrillation and pacing, used in emergency resuscitation settings to deliver synchronized electrical shocks and pacing stimuli to restore normal heart rhythms.
The TIGER PULSE is classified as a Class II device under FDA regulations and is authorised via the 510(k) clearance process. The company is based in the United States.
Catalogue
Tiger Pulse Ref K830325
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bertone & Assoc. have in the registry?
The registry currently lists 1 device for Bertone & Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bertone & Assoc.'s devices?
Among its 1 most recently registered device, Bertone & Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bertone & Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bertone & Assoc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bertone & Assoc. in the registry?
The most recently registered devices listed for Bertone & Assoc. include TIGER PULSE.