Diatek Instruments, Inc.
Country not established
- Devices
- 1
What Diatek Instruments, Inc. makes
Diatek Instruments, Inc. manufactures the SURETEMP, a medical device designed for temperature monitoring and measurement in clinical settings.
The SURETEMP falls under FDA Class II regulation and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Suretemp Ref K964643
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Diatek Instruments, Inc. have in the registry?
The registry currently lists 1 device for Diatek Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diatek Instruments, Inc.'s devices?
Among its 1 most recently registered device, Diatek Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Diatek Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Diatek Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Diatek Instruments, Inc. in the registry?
The most recently registered devices listed for Diatek Instruments, Inc. include SURETEMP.