London Rubber Co. (India), Ltd.
IndiaFDA applicant, unverified
- Devices
- 1
What London Rubber Co. (India), Ltd. makes
London Rubber Co. (India), Ltd. manufactures multiple latex patient examination gloves designed for medical and clinical use, ensuring barrier protection during examinations and procedures.
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
Multiple Latex Patient Examination Gloves Ref K914049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does London Rubber Co. (India), Ltd. have in the registry?
The registry currently lists 1 device for London Rubber Co. (India), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list London Rubber Co. (India), Ltd.'s devices?
Among its 1 most recently registered device, London Rubber Co. (India), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do London Rubber Co. (India), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for London Rubber Co. (India), Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from London Rubber Co. (India), Ltd. in the registry?
The most recently registered devices listed for London Rubber Co. (India), Ltd. include MULTIPLE LATEX PATIENT EXAMINATION GLOVES.