Mechanical Application Designs, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Lift Master Ref K972563
Regimes: 510(k) Registry: 510(k)TK40 - Tiltmaster Ref K961744
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mechanical Application Designs, Inc. have in the registry?
The registry currently lists 3 devices for Mechanical Application Designs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mechanical Application Designs, Inc.'s devices?
Among its 3 most recently registered devices, Mechanical Application Designs, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mechanical Application Designs, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mechanical Application Designs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mechanical Application Designs, Inc. in the registry?
The most recently registered devices listed for Mechanical Application Designs, Inc. include TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT, LIFT MASTER and TK40 - TILTMASTER.