510(k) K131598
K131598 is an FDA 510(k) premarket notification submitted by United States Endoscopy Group, Inc. for the device "ANAL RECTAL OVERTUBE". The FDA issued a decision of Substantially Equivalent on February 26, 2014. The device falls under product code FED (Endoscopic Access Overtube, Gastroenterology-Urology), a Class II device regulated under 21 CFR 876.1500. United States Endoscopy Group, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 26, 2014
- Date Received
- June 3, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscopic Access Overtube, Gastroenterology-Urology
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
To facilitate passage and aid advancement of endoscopes into the body, especially in cases of repeated intubation.