Zetek, Inc.
Country not established
- Devices
- 1
What Zetek, Inc. makes
Zetek, Inc. manufactures the CUE Fertility Monitor, a device designed to track ovulation and menstrual cycle patterns for fertility awareness.
The CUE Fertility Monitor is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Cue Fertility Monitor Ref K850579
510(k) 510(k)
Frequently asked questions
How many devices does Zetek, Inc. have in the registry?
The registry currently lists 1 device for Zetek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zetek, Inc.'s devices?
Among its 1 most recently registered device, Zetek, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Zetek, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zetek, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zetek, Inc. in the registry?
The most recently registered devices listed for Zetek, Inc. include CUE FERTILITY MONITOR.