Gastric Lightguide (GLG)
K-Number: K212407 · 2022-07-26
ApplicantNaser Dib Gabinet Lekarksi Nasmed
Decision Date2022-07-26
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Gastric Lightguide (GLG) is a medical device manufactured by Naser Dib Gabinet Lekarksi Nasmed. It received FDA 510(k) clearance on 2022-07-26 under approval number K212407. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Naser Dib Gabinet Lekarksi Nasmed. The 510(k) number is K212407.
When was Gastric Lightguide (GLG) approved by the FDA?
Gastric Lightguide (GLG) received FDA 510(k) clearance on 2022-07-26, under approval number K212407.
What company makes Gastric Lightguide (GLG)?
Gastric Lightguide (GLG) is manufactured by Naser Dib Gabinet Lekarksi Nasmed.
What is the FDA product code for Gastric Lightguide (GLG)?
The FDA product code for Gastric Lightguide (GLG) is KNT.
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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.