Hytek Medical, Inc.
Country not established
- Devices
- 1
What Hytek Medical, Inc. makes
Hytek Medical, Inc. manufactures the sOLVe Tube, which is a Class II medical device.
The company is based in the US and its products are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
sOLVe Tube Ref K201026
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hytek Medical, Inc. have in the registry?
The registry currently lists 1 device for Hytek Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hytek Medical, Inc.'s devices?
Among its 1 most recently registered device, Hytek Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hytek Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hytek Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hytek Medical, Inc. in the registry?
The most recently registered devices listed for Hytek Medical, Inc. include sOLVe Tube.