Core-M, L.P.
Country not established
- Devices
- 1
What Core-M, L.P. makes
Core-M, L.P. manufactures the FI02 Sensing Module, a device designed for monitoring and detecting specific physiological or environmental parameters in medical or industrial applications. This module integrates sensing technology to provide real-time data collection and signal processing for use in diagnostic or operational settings.
The FI02 Sensing Module is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States, where its products are subject to compliance with U.S. medical device authorization requirements.
Catalogue
FI02 Sensing Module Ref K944120
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Core-M, L.P. have in the registry?
The registry currently lists 1 device for Core-M, L.P.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Core-M, L.P.'s devices?
Among its 1 most recently registered device, Core-M, L.P. has devices listed in FDA 510(k) (1 device).
What risk classes do Core-M, L.P.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Core-M, L.P.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Core-M, L.P. in the registry?
The most recently registered devices listed for Core-M, L.P. include FI02 SENSING MODULE.