Murex Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Murex Diagnostics, Inc. makes
Murex Diagnostics, Inc. manufactures in vitro diagnostic devices including the MUREX RUB-EX and WELLCOLEX E-COLI OI57 ZC60 test kits.
These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Murex Rub-Ex Ref K954920
Regimes: 510(k) Registry: 510(k)Wellcolex E-Coli OI57 ZC60 Ref K962028
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Murex Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Murex Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Murex Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Murex Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Murex Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Murex Diagnostics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Murex Diagnostics, Inc. in the registry?
The most recently registered devices listed for Murex Diagnostics, Inc. include MUREX RUB-EX and WELLCOLEX E-COLI OI57 ZC60.