Tegas Setia Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 1
What Tegas Setia Sdn Bhd makes
Tegas Setia Sdn Bhd makes patient examination gloves made of latex.
The company's devices are classified as Class I and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892299
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tegas Setia Sdn Bhd have in the registry?
The registry currently lists 1 device for Tegas Setia Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tegas Setia Sdn Bhd's devices?
Among its 1 most recently registered device, Tegas Setia Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Tegas Setia Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tegas Setia Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tegas Setia Sdn Bhd in the registry?
The most recently registered devices listed for Tegas Setia Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).