Equal Diagnostics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Equal Diagnostics, Inc. makes
Equal Diagnostics, Inc. manufactures in vitro diagnostic reagents, specifically the Sentinel Cholinesterase Liquid and Sentinel Lipase Liquid assays.
The company is based in the United States, and its product portfolio includes Class I and Class II medical devices that are listed in the FDA 510(k) registry.
Catalogue
- 510(k) 510(k)
Sentinel Lipase Liquid Model 17.401B Ref K961179
510(k) 510(k)
Frequently asked questions
How many devices does Equal Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Equal Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Equal Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Equal Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Equal Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Equal 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 Equal Diagnostics, Inc. in the registry?
The most recently registered devices listed for Equal Diagnostics, Inc. include SENTINEL CHOLINESTERASE LIQUID MODEL NUMBER 17.019A & 17.606 and SENTINEL LIPASE LIQUID MODEL 17.401B.