Vollrath Group, Inc.
Country not established
- Devices
- 1
Catalogue
Patient Examination Gloves (Latex) Ref K892683
510(k) 510(k)
Frequently asked questions
How many devices does Vollrath Group, Inc. have in the registry?
The registry currently lists 1 device for Vollrath Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vollrath Group, Inc.'s devices?
Among its 1 most recently registered device, Vollrath Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Vollrath Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vollrath Group, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vollrath Group, Inc. in the registry?
The most recently registered devices listed for Vollrath Group, Inc. include PATIENT EXAMINATION GLOVES (LATEX).