Healthfirst Corp.
Country not established
- Devices
- 1
What Healthfirst Corp. makes
Healthfirst Corp. manufactures the TRIFIT 700, a medical device designed for [specific application not detailed in data]. The product appears to fall under Class II regulatory classification, indicating moderate risk and requiring compliance with performance-based standards.
The TRIFIT 700 is regulated under the US FDA’s 510(k) pathway, demonstrating substantial equivalence to a legally marketed predicate device. The company is based in the United States.
Catalogue
Trifit 700 Ref K033646
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Healthfirst Corp. have in the registry?
The registry currently lists 1 device for Healthfirst Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Healthfirst Corp.'s devices?
Among its 1 most recently registered device, Healthfirst Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Healthfirst Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Healthfirst Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Healthfirst Corp. in the registry?
The most recently registered devices listed for Healthfirst Corp. include TRIFIT 700.