Sakers, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sakers, Inc. makes
Sakers, Inc. manufactures rapid diagnostic devices, including the CRACK-IT CHAP SCREEN for detecting chlamydia and the CRACK-IT CANNABINOID SCREEN for identifying cannabinoid compounds in 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
Crack-It Chap Screen Ref K874389
Regimes: 510(k) Registry: 510(k)Crack-It Cannabinoid Screen Ref K874390
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sakers, Inc. have in the registry?
The registry currently lists 2 devices for Sakers, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sakers, Inc.'s devices?
Among its 2 most recently registered devices, Sakers, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sakers, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sakers, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sakers, Inc. in the registry?
The most recently registered devices listed for Sakers, Inc. include CRACK-IT CHAP SCREEN and CRACK-IT CANNABINOID SCREEN.