Xtrana, Inc.
Country not established
- Devices
- 1
What Xtrana, Inc. makes
Xtrana, Inc. makes the AUTODIMER ASSAY MODEL # 1431, which is a diagnostic test device used to detect dimerization in biological samples.
The AUTODIMER ASSAY MODEL # 1431 is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Autodimer Assay Model # 1431 Ref K012755
510(k) 510(k)
Frequently asked questions
How many devices does Xtrana, Inc. have in the registry?
The registry currently lists 1 device for Xtrana, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xtrana, Inc.'s devices?
Among its 1 most recently registered device, Xtrana, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Xtrana, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Xtrana, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xtrana, Inc. in the registry?
The most recently registered devices listed for Xtrana, Inc. include AUTODIMER ASSAY MODEL # 1431.