Hmicro, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Hmicro, Inc. makes
Hmicro, Inc. manufactures wired C-Patch electrodes for medical monitoring, including the HMICRO WIRED C-PATCH ELECTRODE, and a biosensor system combining the LifeSignals WiPatch with an iOS-compatible receiver and app (LifeSignals WiPoint Biosensor_iOS Receiver_App System). These products are designed for physiological signal acquisition and wireless data transmission.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. Hmicro, Inc. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System) Ref K172011
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hmicro, Inc. have in the registry?
The registry currently lists 2 devices for Hmicro, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hmicro, Inc.'s devices?
Among its 2 most recently registered devices, Hmicro, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hmicro, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hmicro, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hmicro, Inc. in the registry?
The most recently registered devices listed for Hmicro, Inc. include HMICRO WIRED C-PATCH ELECTRODE, TRADE NAME SUBJECT TO CHANGE and LifeSignals WiPoint Biosensor_iOS Receiver_App System (LifeSignals WiPatch & WiApp System).