Chesire Laboratories
Country not established
- Devices
- 4
What Chesire Laboratories makes
Chesire Laboratories manufactures medical devices including mid-stream collection sets, sterile suction catheters with control, and latex examination gloves (both powdered and powder-free).
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Chesire Laboratories is based in the US.
Catalogue
Mid-Stream Collection Set Ref K770231
Regimes: 510(k) Registry: 510(k)Sterile Suction Catheter W/Control Ref K770233
Regimes: 510(k) Registry: 510(k)Doctor's Choice Latex Examination Gloves Ref K924265
Regimes: 510(k) Registry: 510(k)Doctor's Choice Powder Free Latex Exam Gloves Ref K924266
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chesire Laboratories have in the registry?
The registry currently lists 4 devices for Chesire Laboratories. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chesire Laboratories's devices?
Among its 4 most recently registered devices, Chesire Laboratories has devices listed in FDA 510(k) (4 devices).
What risk classes do Chesire Laboratories's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Chesire Laboratories's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chesire Laboratories in the registry?
The most recently registered devices listed for Chesire Laboratories include MID-STREAM COLLECTION SET, STERILE SUCTION CATHETER W/CONTROL, DOCTOR'S CHOICE LATEX EXAMINATION GLOVES and DOCTOR'S CHOICE POWDER FREE LATEX EXAM GLOVES.