Keithley Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Keithley Instruments, Inc. makes
Keithley Instruments, Inc. manufactures medical radiation measurement devices, including the TN-RD-50 dosimeter for advanced therapy monitoring and the Model 35300 Tracker™ Therapy Beam Evaluator for beam quality assessment. Their portfolio also includes the Keithley Model 75100 and 75200 systems, designed for precise radiation dose tracking in clinical settings.
These devices fall under FDA Class II regulation and are authorised via the 510(k) pathway. The company is headquartered in the United States, with its products listed in the FDA’s 510(k) registry.
Catalogue
Tn-Rd-50 Ref K932598
Regimes: 510(k) Registry: 510(k)Advanced Therapy Dosimeter Ref K942083
Regimes: 510(k) Registry: 510(k)Model 35300 Tracker(Tm) Therapy Beam Evaluator Ref K874893
Regimes: 510(k) Registry: 510(k)Keithley Model 75100 & 75200 Ref K854110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Keithley Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Keithley Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Keithley Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Keithley Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Keithley Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Keithley Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Keithley Instruments, Inc. in the registry?
The most recently registered devices listed for Keithley Instruments, Inc. include TN-RD-50, ADVANCED THERAPY DOSIMETER, MODEL 35300 TRACKER(TM) THERAPY BEAM EVALUATOR and KEITHLEY MODEL 75100 & 75200.