American Advisors, Inc.
Country not established
- Devices
- 1
What American Advisors, Inc. makes
American Advisors, Inc. manufactures sterile surgical gloves, including double-glove systems designed for use in operating rooms and clinical settings. These products are intended to provide an additional barrier to reduce contamination risk during surgical procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, with relevant products listed via the 510(k) pathway. These devices are distributed in the United States, where the manufacturer is based.
Catalogue
Sterile Surgical Gloves/Double Glover Ref K905012
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Advisors, Inc. have in the registry?
The registry currently lists 1 device for American Advisors, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Advisors, Inc.'s devices?
Among its 1 most recently registered device, American Advisors, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do American Advisors, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for American Advisors, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from American Advisors, Inc. in the registry?
The most recently registered devices listed for American Advisors, Inc. include STERILE SURGICAL GLOVES/DOUBLE GLOVER.