Cheshire Diagnostics, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 6
What Cheshire Diagnostics, Ltd. makes
Cheshire Diagnostics, Ltd. manufactures in vitro diagnostic ELISA kits for detecting IgG and IgM antibodies. The kits include both HRP-conjugated and non-conjugated variants for specific antigen tests, designed for laboratory use in serological analysis.
These products are classified as Class II devices under FDA regulations and are authorised via 510(k) clearance. The company is based in the United States and its devices are listed in the FDA’s 510(k) registry.
Catalogue
QAB2A Igg Elisa Kit Hrp Ref K021611
Regimes: 510(k) Registry: 510(k)QAB2A Igg Elisa Kit Ref K020695
Regimes: 510(k) Registry: 510(k)Qaca Igg/Igm Elisa Kit Hrp Ref K021192
Regimes: 510(k) Registry: 510(k)QAB2A Igm Elisa Kit Hrp Ref K021610
Regimes: 510(k) Registry: 510(k)QAB2A Igm Elisa Kit Ref K020694
Regimes: 510(k) Registry: 510(k)Qaca Igg/Igm Elisa Kit Ref K020241
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cheshire Diagnostics, Ltd. have in the registry?
The registry currently lists 6 devices for Cheshire Diagnostics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cheshire Diagnostics, Ltd.'s devices?
Among its 6 most recently registered devices, Cheshire Diagnostics, Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Cheshire Diagnostics, Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Cheshire Diagnostics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cheshire Diagnostics, Ltd. in the registry?
The most recently registered devices listed for Cheshire Diagnostics, Ltd. include QAB2A IGG ELISA KIT HRP, QAB2A IGG ELISA KIT, QACA IGG/IGM ELISA KIT HRP and QAB2A IGM ELISA KIT HRP.