Ku Shing Industries Sdn. Bhd.
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Ku Shing Industries Sdn. Bhd. makes
Ku Shing Industries Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These products are classified as Class I devices under FDA regulations and are recorded in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891936
510(k) 510(k)
Frequently asked questions
How many devices does Ku Shing Industries Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Ku Shing Industries Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ku Shing Industries Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Ku Shing Industries Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ku Shing Industries Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ku Shing Industries Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ku Shing Industries Sdn. Bhd. in the registry?
The most recently registered devices listed for Ku Shing Industries Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).