Sequitur Health Corp.
United Statesfrom the FDA registration address FDA establishment FEI 3023591031
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AMI™ Plasma Cartridge, AMI™ Ref K260613
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3023591031
- Address
- 6161 E Mayo Blvd, Phoenix, AZ, 85054
Frequently asked questions
How many devices does SEQUITUR HEALTH CORP. have in the registry?
The registry currently lists 1 device for SEQUITUR HEALTH CORP.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SEQUITUR HEALTH CORP.'s devices?
Among its 1 most recently registered device, SEQUITUR HEALTH CORP. has devices listed in FDA 510(k) (1 device).
What risk classes do SEQUITUR HEALTH CORP.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for SEQUITUR HEALTH CORP.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SEQUITUR HEALTH CORP. in the registry?
The most recently registered devices listed for SEQUITUR HEALTH CORP. include AMI™ Plasma Cartridge, AMI™.