American Laboratories, Inc.
Country not established
- Devices
- 1
What American Laboratories, Inc. makes
American Laboratories, Inc. manufactures condoms under the DUET brand, designed for contraceptive protection during sexual intercourse.
The DUET condom is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Duet (Condoms) Ref K880185
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Laboratories, Inc. have in the registry?
The registry currently lists 1 device for American Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Laboratories, Inc.'s devices?
Among its 1 most recently registered device, American Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Laboratories, Inc. in the registry?
The most recently registered devices listed for American Laboratories, Inc. include DUET (CONDOMS).