Genie Rubber Products Co.
Country not established
- Devices
- 1
What Genie Rubber Products Co. makes
Genie Rubber Products Co. makes patient examination gloves made of latex.
The company's devices are classified as Class I and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891267
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genie Rubber Products Co. have in the registry?
The registry currently lists 1 device for Genie Rubber Products Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genie Rubber Products Co.'s devices?
Among its 1 most recently registered device, Genie Rubber Products Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Genie Rubber Products Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Genie Rubber Products Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Genie Rubber Products Co. in the registry?
The most recently registered devices listed for Genie Rubber Products Co. include PATIENT EXAMINATION GLOVES (LATEX).