Votra (Malaysia) Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
What Votra (Malaysia) Sdn Bhd makes
Votra (Malaysia) Sdn Bhd manufactures latex patient examination gloves, designed for single-use medical procedures and clinical examinations.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892029
510(k) 510(k)
Frequently asked questions
How many devices does Votra (Malaysia) Sdn Bhd have in the registry?
The registry currently lists 1 device for Votra (Malaysia) Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Votra (Malaysia) Sdn Bhd's devices?
Among its 1 most recently registered device, Votra (Malaysia) Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Votra (Malaysia) Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Votra (Malaysia) Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Votra (Malaysia) Sdn Bhd in the registry?
The most recently registered devices listed for Votra (Malaysia) Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).