Pro-Tex Products, Inc.
Country not established
- Devices
- 1
What Pro-Tex Products, Inc. makes
Pro-Tex Products, Inc. manufactures patient examination gloves, designed for single-use clinical procedures to maintain hygiene and reduce infection risk.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K894121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro-Tex Products, Inc. have in the registry?
The registry currently lists 1 device for Pro-Tex Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro-Tex Products, Inc.'s devices?
Among its 1 most recently registered device, Pro-Tex Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pro-Tex Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pro-Tex Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pro-Tex Products, Inc. in the registry?
The most recently registered devices listed for Pro-Tex Products, Inc. include PATIENT EXAMINATION GLOVES.