Makromed, Inc.
United Statesfrom the FDA registration address FDA FEI 3029464335
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cloudekg Ref K130878
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3029464335
- Address
- 88 STILES ROAD, Salem, NH, 03079
Frequently asked questions
How many devices does Makromed, Inc. have in the registry?
The registry currently lists 1 device for Makromed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Makromed, Inc.'s devices?
Among its 1 most recently registered device, Makromed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Makromed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Makromed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Makromed, Inc. in the registry?
The most recently registered devices listed for Makromed, Inc. include CLOUDEKG.