C & S Microinstruments, Ltd.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What C & S Microinstruments, Ltd. makes
C & S Microinstruments, Ltd. manufactures the ENDOBRUSH, a device designed for endoscopic procedures to collect tissue samples or debris from internal body cavities or ducts.
The ENDOBRUSH is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Endobrush Ref K870177
510(k) 510(k)
Frequently asked questions
How many devices does C & S Microinstruments, Ltd. have in the registry?
The registry currently lists 1 device for C & S Microinstruments, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C & S Microinstruments, Ltd.'s devices?
Among its 1 most recently registered device, C & S Microinstruments, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do C & S Microinstruments, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for C & S Microinstruments, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from C & S Microinstruments, Ltd. in the registry?
The most recently registered devices listed for C & S Microinstruments, Ltd. include ENDOBRUSH.