Instrument Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Instrument Technology, Inc. makes
Instrument Technology, Inc. manufactures the COMBISCOPE, a diagnostic imaging device for medical examinations, and the ITI 200 Electric Motor Drive, a universal wheelchair accessory for mobility assistance.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Combiscope Ref K852655
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Instrument Technology, Inc. have in the registry?
The registry currently lists 2 devices for Instrument Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Instrument Technology, Inc.'s devices?
Among its 2 most recently registered devices, Instrument Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Instrument Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Instrument Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Instrument Technology, Inc. in the registry?
The most recently registered devices listed for Instrument Technology, Inc. include COMBISCOPE and ITI 200 ELECTRIC MOTOR DRIVE, UNIV.-WHEELCHAIR ACC.