Asian Latex, Ltd.
IndiaFDA applicant, unverified
- Devices
- 1
What Asian Latex, Ltd. makes
Asian Latex, Ltd. manufactures patient examination gloves, designed for single-use medical and clinical procedures to maintain hygiene and reduce infection risk.
These products 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 Ref K910442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asian Latex, Ltd. have in the registry?
The registry currently lists 1 device for Asian Latex, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asian Latex, Ltd.'s devices?
Among its 1 most recently registered device, Asian Latex, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Asian Latex, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Asian Latex, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Asian Latex, Ltd. in the registry?
The most recently registered devices listed for Asian Latex, Ltd. include PATIENT EXAMINATION GLOVES.