Chung Yang Rubber Works (M) Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Chung Yang Rubber Works (M) Sdn. Bhd. makes
The company manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892782
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chung Yang Rubber Works (M) Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Chung Yang Rubber Works (M) Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chung Yang Rubber Works (M) Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Chung Yang Rubber Works (M) Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Chung Yang Rubber Works (M) Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Chung Yang Rubber Works (M) Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Chung Yang Rubber Works (M) Sdn. Bhd. in the registry?
The most recently registered devices listed for Chung Yang Rubber Works (M) Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).