Medcraft Corp.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Comp-Act Iv Ref K791795
Regimes: 510(k) Registry: 510(k)Accutape 24 Ref K760508
Regimes: 510(k) Registry: 510(k)Treadmill, Diagnostic Ref K760509
Regimes: 510(k) Registry: 510(k)Electroshock Unit Neurology Model B-25 Ref K860467
Regimes: 510(k) Registry: 510(k)Monitoring System, Rehabilitation Ref K760510
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medcraft Corp. have in the registry?
The registry currently lists 5 devices for Medcraft Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medcraft Corp.'s devices?
Among its 5 most recently registered devices, Medcraft Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medcraft Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medcraft Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medcraft Corp. in the registry?
The most recently registered devices listed for Medcraft Corp. include COMP-ACT IV, ACCUTAPE 24, TREADMILL, DIAGNOSTIC and ELECTROSHOCK UNIT NEUROLOGY MODEL B-25.