Alicia Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Alicia Diagnostics, Inc. makes
Alicia Diagnostics, Inc. manufactures automated cell counters, including the GENESIS I and its modified version, designed for laboratory use to quantify and analyze cell samples.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Genesis I Automated Cell Counter Ref K910679
Regimes: 510(k) Registry: 510(k)Genesis 1, Automated Cell Counter, Modification Ref K925909
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alicia Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Alicia Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alicia Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Alicia Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alicia Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alicia Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alicia Diagnostics, Inc. in the registry?
The most recently registered devices listed for Alicia Diagnostics, Inc. include GENESIS I AUTOMATED CELL COUNTER and GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION.