Alberto-Culver USA, Inc.
Country not established
- Devices
- 1
What Alberto-Culver USA, Inc. makes
Alberto-Culver USA, Inc. manufactures intimate lubricants, including the FDS Intimate and Intimate Warming Lubricant, designed for personal use.
These products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database.
Catalogue
Fds Intimate And Intimate Warming Lubricant Ref K060145
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alberto-Culver USA, Inc. have in the registry?
The registry currently lists 1 device for Alberto-Culver USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alberto-Culver USA, Inc.'s devices?
Among its 1 most recently registered device, Alberto-Culver USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alberto-Culver USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alberto-Culver USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alberto-Culver USA, Inc. in the registry?
The most recently registered devices listed for Alberto-Culver USA, Inc. include FDS INTIMATE AND INTIMATE WARMING LUBRICANT.