Ampcor Diagnostics, Inc.
Country not established
- Devices
- 1
What Ampcor Diagnostics, Inc. makes
Ampcor Diagnostics, Inc. manufactures liquid controls for syphilis testing, specifically the RPR (rapid plasma reagin) assay, used to verify the accuracy of diagnostic tests for syphilis.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway in the United States.
Catalogue
Adi Syphilis Rpr Liquid Controls Ref K980638
510(k) 510(k)
Frequently asked questions
How many devices does Ampcor Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Ampcor Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ampcor Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Ampcor Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ampcor Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ampcor Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ampcor Diagnostics, Inc. in the registry?
The most recently registered devices listed for Ampcor Diagnostics, Inc. include ADI SYPHILIS RPR LIQUID CONTROLS.