Kosel Industries Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Kosel Industries Sdn Bhd makes
Kosel Industries Sdn Bhd manufactures latex patient examination gloves, designed for clinical use during medical procedures to ensure sterility and reduce infection risk.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891937
510(k) 510(k)
Frequently asked questions
How many devices does Kosel Industries Sdn Bhd have in the registry?
The registry currently lists 1 device for Kosel Industries Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kosel Industries Sdn Bhd's devices?
Among its 1 most recently registered device, Kosel Industries Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Kosel Industries Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kosel Industries Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kosel Industries Sdn Bhd in the registry?
The most recently registered devices listed for Kosel Industries Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).