Indevr, Inc.
Country not established
- Devices
- 1
What Indevr, Inc. makes
Indevr, Inc. manufactures the FluChip-8G Influenza A+B Assay, a diagnostic device designed to detect and differentiate between Influenza A and B viruses in clinical samples.
The FluChip-8G Influenza A+B Assay is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
FluChip-8G Influenza A+B Assay Ref K182513
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Indevr, Inc. have in the registry?
The registry currently lists 1 device for Indevr, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Indevr, Inc.'s devices?
Among its 1 most recently registered device, Indevr, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Indevr, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Indevr, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Indevr, Inc. in the registry?
The most recently registered devices listed for Indevr, Inc. include FluChip-8G Influenza A+B Assay.