Lit Seng Development Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Lit Seng Development Sdn. Bhd. makes
Lit Seng Development Sdn. Bhd. manufactures patient examination gloves, a sterile barrier device used during medical procedures to 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 US.
Catalogue
Patient Examination Gloves Ref K895617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lit Seng Development Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Lit Seng Development Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lit Seng Development Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Lit Seng Development Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Lit Seng Development Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lit Seng Development Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lit Seng Development Sdn. Bhd. in the registry?
The most recently registered devices listed for Lit Seng Development Sdn. Bhd. include PATIENT EXAMINATION GLOVES.