510(k) K212407
K212407 is an FDA 510(k) premarket notification submitted by Naser Dib Gabinet Lekarksi Nasmed for the device "Gastric Lightguide (GLG)". The FDA issued a decision of Substantially Equivalent on Jul 26, 2022. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 26, 2022
- Date Received
- Aug 3, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tubes, Gastrointestinal (And Accessories)
- Device Class
- Class II
- Regulation Number
- 876.5980
- Review Panel
- GU
- Submission Type
- 510(k)