Hawksley & Sons, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Hawksley & Sons, Ltd. makes
Hawksley & Sons, Ltd. manufactures the MICRO HAEMATOCRIT CENTRIFUGE, a Class II medical device used for hematocrit determination.
The company is based in the US, and its products are listed in the FDA 510(k) registry, which regulates Class II devices that require special controls to ensure safety and effectiveness.
Catalogue
Micro Haematocrit Centrifuge Ref K960491
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hawksley & Sons, Ltd. have in the registry?
The registry currently lists 1 device for Hawksley & Sons, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hawksley & Sons, Ltd.'s devices?
Among its 1 most recently registered device, Hawksley & Sons, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hawksley & Sons, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hawksley & Sons, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hawksley & Sons, Ltd. in the registry?
The most recently registered devices listed for Hawksley & Sons, Ltd. include MICRO HAEMATOCRIT CENTRIFUGE.