Naser Dib Gabinet Lekarksi Nasmed
PolandFDA 510(k) applicant, unverified
- Devices
- 1
What Naser Dib Gabinet Lekarksi Nasmed makes
The company manufactures the Gastric Lightguide (GLG), a device designed for endoscopic illumination within the gastrointestinal tract to enhance visualization during procedures.
The Gastric Lightguide is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Gastric Lightguide (GLG) Ref K212407
510(k) 510(k)
Frequently asked questions
How many devices does Naser Dib Gabinet Lekarksi Nasmed have in the registry?
The registry currently lists 1 device for Naser Dib Gabinet Lekarksi Nasmed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Naser Dib Gabinet Lekarksi Nasmed's devices?
Among its 1 most recently registered device, Naser Dib Gabinet Lekarksi Nasmed has devices listed in FDA 510(k) (1 device).
What risk classes do Naser Dib Gabinet Lekarksi Nasmed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Naser Dib Gabinet Lekarksi Nasmed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Naser Dib Gabinet Lekarksi Nasmed in the registry?
The most recently registered devices listed for Naser Dib Gabinet Lekarksi Nasmed include Gastric Lightguide (GLG).