Viratect, Inc.
Country not established
- Devices
- 1
What Viratect, Inc. makes
Viratect, Inc. manufactures patient examination gloves, designed for use in clinical settings to maintain hygiene and reduce contamination during medical procedures.
These products fall under FDA Class I devices and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K892961
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Viratect, Inc. have in the registry?
The registry currently lists 1 device for Viratect, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Viratect, Inc.'s devices?
Among its 1 most recently registered device, Viratect, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Viratect, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Viratect, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Viratect, Inc. in the registry?
The most recently registered devices listed for Viratect, Inc. include PATIENT EXAMINATION GLOVES.