Armstrong Laboratories, Inc.
Country not established
- Devices
- 1
What Armstrong Laboratories, Inc. makes
Armstrong Laboratories, Inc. manufactures sterile saline solutions, which are sterile isotonic sodium chloride solutions used for intravenous infusion, wound irrigation, or other medical applications requiring a physiologically balanced fluid.
The company’s sterile saline solutions are classified as Class II medical devices under FDA regulations and are listed under the Premarket Approval (PMA) pathway. The manufacturer operates from the United States.
Catalogue
Armstrong Sterile Saline Solution Ref P870058
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Armstrong Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Armstrong Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Armstrong Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Armstrong Laboratories, Inc. has devices listed in FDA PMA (1 device).
What risk classes do Armstrong Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Armstrong Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Armstrong Laboratories, Inc. in the registry?
The most recently registered devices listed for Armstrong Laboratories, Inc. include ARMSTRONG STERILE SALINE SOLUTION.