510(k) K210437

Standard Bougie, 38 Fr. by Standard Bariatrics — Product Code KNT

K210437 is an FDA 510(k) premarket notification submitted by Standard Bariatrics for the device "Standard Bougie, 38 Fr.". The FDA issued a decision of Substantially Equivalent on June 29, 2021. The device falls under product code KNT (Tubes, Gastrointestinal (And Accessories)), a Class II device regulated under 21 CFR 876.5980. Standard Bariatrics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 29, 2021
Date Received
February 12, 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