Industri Getah Jacon
MalaysiaFDA applicant, unverified
- Devices
- 1
What Industri Getah Jacon makes
Industri Getah Jacon manufactures patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
The company’s portfolio is regulated under FDA’s Class I device classification, with products listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Patient Examination Glove Ref K890593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Industri Getah Jacon have in the registry?
The registry currently lists 1 device for Industri Getah Jacon. Devices recorded under merged duplicate company entries are counted once.
Which registries list Industri Getah Jacon's devices?
Among its 1 most recently registered device, Industri Getah Jacon has devices listed in FDA 510(k) (1 device).
What risk classes do Industri Getah Jacon's devices fall under?
Among its 1 most recently registered device, the classes recorded for Industri Getah Jacon's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Industri Getah Jacon in the registry?
The most recently registered devices listed for Industri Getah Jacon include PATIENT EXAMINATION GLOVE.