J-Tech, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
Catalogue
Inclinometer Ref K954647
510(k) 510(k)- 510(k) 510(k)
Jtech 50 Series Cutting Loop Ref K913587
510(k) 510(k)Gs-220 Hand Impairment Evaluation System Ref K912526
510(k) 510(k)Large Muscle Strength Gauge Ref K945630
510(k) 510(k)
Frequently asked questions
How many devices does J-Tech, Inc. have in the registry?
The registry currently lists 5 devices for J-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list J-Tech, Inc.'s devices?
Among its 5 most recently registered devices, J-Tech, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do J-Tech, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for J-Tech, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from J-Tech, Inc. in the registry?
The most recently registered devices listed for J-Tech, Inc. include INCLINOMETER, SURFACE ELECTROMYOGRAPH BIOFEEDBACK MUSCLE ACTIVITY DEVICE, JTECH 50 SERIES CUTTING LOOP and GS-220 HAND IMPAIRMENT EVALUATION SYSTEM.