Gastric Lightguide (GLG)
K-Number: K212407 · 2022-07-26
Device Summary
Frequently Asked Questions
What is the Gastric Lightguide (GLG)?
Gastric Lightguide (GLG) is a medical device that received FDA 510(k) clearance on 2022-07-26. The listed applicant is Naser Dib Gabinet Lekarksi Nasmed. The 510(k) number is K212407.
When did Gastric Lightguide (GLG) receive FDA 510(k) clearance?
Gastric Lightguide (GLG) received FDA 510(k) clearance on 2022-07-26, under 510(k) number K212407.
Who is the listed applicant for Gastric Lightguide (GLG)?
The FDA 510(k) record lists Naser Dib Gabinet Lekarksi Nasmed as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gastric Lightguide (GLG)?
The FDA product code for Gastric Lightguide (GLG) is KNT.
Related Devices (Code: KNT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.