Pmg Medica, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Pmg Medica, Ltd. makes
Pmg Medica, Ltd. makes the BABYCOM device.
The BABYCOM device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Babycom Ref K013547
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pmg Medica, Ltd. have in the registry?
The registry currently lists 1 device for Pmg Medica, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pmg Medica, Ltd.'s devices?
Among its 1 most recently registered device, Pmg Medica, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pmg Medica, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pmg Medica, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pmg Medica, Ltd. in the registry?
The most recently registered devices listed for Pmg Medica, Ltd. include BABYCOM.