Westport Pharmaceuticals, Inc.
Country not established
- Devices
- 1
What Westport Pharmaceuticals, Inc. makes
Westport Pharmaceuticals, Inc. manufactures SALIVART, a medical device designed for the collection and analysis of saliva samples, likely intended for diagnostic or monitoring purposes in clinical settings.
The company’s portfolio is regulated under the FDA’s Premarket Approval (PMA) pathway, with SALIVART classified as a Class U device. The device is listed in the FDA’s regulatory database, and the manufacturer is based in the United States.
Catalogue
Salivart Ref P790016
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Westport Pharmaceuticals, Inc. have in the registry?
The registry currently lists 1 device for Westport Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Westport Pharmaceuticals, Inc.'s devices?
Among its 1 most recently registered device, Westport Pharmaceuticals, Inc. has devices listed in FDA PMA (1 device).
What are the newest devices from Westport Pharmaceuticals, Inc. in the registry?
The most recently registered devices listed for Westport Pharmaceuticals, Inc. include SALIVART.