American Rubber Industries
Country not established
- Devices
- 1
What American Rubber Industries makes
American Rubber Industries manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Latex Patient Examination Gloves Ref K894774
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Rubber Industries have in the registry?
The registry currently lists 1 device for American Rubber Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Rubber Industries's devices?
Among its 1 most recently registered device, American Rubber Industries has devices listed in FDA 510(k) (1 device).
What risk classes do American Rubber Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for American Rubber Industries's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Rubber Industries in the registry?
The most recently registered devices listed for American Rubber Industries include LATEX PATIENT EXAMINATION GLOVES.