Kerala Rubber & Reclaims, Ltd.
IndiaFDA applicant, unverified
- Devices
- 2
What Kerala Rubber & Reclaims, Ltd. makes
Kerala Rubber & Reclaims, Ltd. makes patient examination gloves, including the KRR glove and other patient examination gloves.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patient Examination Glove Ref K933602
Regimes: 510(k) Registry: 510(k)Krr Glove, Patient Examination Gloves Ref K894452
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kerala Rubber & Reclaims, Ltd. have in the registry?
The registry currently lists 2 devices for Kerala Rubber & Reclaims, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kerala Rubber & Reclaims, Ltd.'s devices?
Among its 2 most recently registered devices, Kerala Rubber & Reclaims, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kerala Rubber & Reclaims, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kerala Rubber & Reclaims, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kerala Rubber & Reclaims, Ltd. in the registry?
The most recently registered devices listed for Kerala Rubber & Reclaims, Ltd. include PATIENT EXAMINATION GLOVE and KRR GLOVE, PATIENT EXAMINATION GLOVES.