Jeanine Alcantara Intl.
Country not established
- Devices
- 1
What Jeanine Alcantara Intl. makes
Jeanine Alcantara Intl. manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce contamination risk during clinical examinations.
The company’s latex gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Examination Glove (Latex) Ref K891979
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jeanine Alcantara Intl. have in the registry?
The registry currently lists 1 device for Jeanine Alcantara Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jeanine Alcantara Intl.'s devices?
Among its 1 most recently registered device, Jeanine Alcantara Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Jeanine Alcantara Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jeanine Alcantara Intl.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jeanine Alcantara Intl. in the registry?
The most recently registered devices listed for Jeanine Alcantara Intl. include PATIENT EXAMINATION GLOVE (LATEX).