Stryker GI
Country not established
- Devices
- 1
What Stryker GI makes
Stryker GI manufactures the PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL, a flexible endoscope designed for colonoscopy procedures. This device is intended for visual inspection of the colon and rectum, with a focus on protecting the scope from contamination during withdrawal.
The PROTECTISCOPE CS COLONOSCOPE is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Protectiscope Cs Colonoscope, Non-Intrapull Ref K081004
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker GI have in the registry?
The registry currently lists 1 device for Stryker GI. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker GI's devices?
Among its 1 most recently registered device, Stryker GI has devices listed in FDA 510(k) (1 device).
What risk classes do Stryker GI's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stryker GI's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker GI in the registry?
The most recently registered devices listed for Stryker GI include PROTECTISCOPE CS COLONOSCOPE, NON-INTRAPULL.