Gobo Intl.
Country not established
- Devices
- 1
What Gobo Intl. makes
Gobo Intl. manufactures latex patient examination gloves, designed for clinical use during medical procedures and examinations.
These gloves are classified as Class I devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry.
Catalogue
Patient Examination Gloves (Latex) Ref K892633
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gobo Intl. have in the registry?
The registry currently lists 1 device for Gobo Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gobo Intl.'s devices?
Among its 1 most recently registered device, Gobo Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Gobo Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gobo Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gobo Intl. in the registry?
The most recently registered devices listed for Gobo Intl. include PATIENT EXAMINATION GLOVES (LATEX).