Equimed Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Equimed Corp. makes
Equimed Corp. manufactures ECG transmitters, including the VITEL III and its CM variant, designed for wireless monitoring of cardiac electrical activity.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Vitel Iii, Ecg Transmitter Ref K872229
510(k) 510(k)Vitel Iii Cm Ref K880533
510(k) 510(k)
Frequently asked questions
How many devices does Equimed Corp. have in the registry?
The registry currently lists 2 devices for Equimed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Equimed Corp.'s devices?
Among its 2 most recently registered devices, Equimed Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Equimed Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Equimed Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Equimed Corp. in the registry?
The most recently registered devices listed for Equimed Corp. include VITEL III, ECG TRANSMITTER and VITEL III CM.