Myriad Genetic Laboratories
United Statesfrom the FDA registration address FDA FEI 3030654068
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bracanalysis Cdx Ref P140020
Regimes: PMA Registry: PMA
Company details
- FDA FEI number
- 3030654068
- Address
- 322 N 2200 W, Salt Lake City, UT, 84116
Frequently asked questions
How many devices does Myriad Genetic Laboratories have in the registry?
The registry currently lists 1 device for Myriad Genetic Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Myriad Genetic Laboratories's devices?
Among its 1 most recently registered device, Myriad Genetic Laboratories has devices listed in FDA PMA (1 device).
What risk classes do Myriad Genetic Laboratories's devices fall under?
Among its 1 most recently registered device, the classes recorded for Myriad Genetic Laboratories's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Myriad Genetic Laboratories in the registry?
The most recently registered devices listed for Myriad Genetic Laboratories include BRACANALYSIS CDX.