Lifemed Technologies, Inc.
Country not established
- Devices
- 1
What Lifemed Technologies, Inc. makes
Lifemed Technologies, Inc. manufactures the LIFE PAC, a medical device designed for external cardiac monitoring and defibrillation, used in emergency and pre-hospital settings to support cardiac arrest response and arrhythmia management.
The LIFE PAC is classified as a Class I device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Life Pac Ref K854807
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifemed Technologies, Inc. have in the registry?
The registry currently lists 1 device for Lifemed Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifemed Technologies, Inc.'s devices?
Among its 1 most recently registered device, Lifemed Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lifemed Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifemed Technologies, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lifemed Technologies, Inc. in the registry?
The most recently registered devices listed for Lifemed Technologies, Inc. include LIFE PAC.