510(k) K201121
K201121 is an FDA 510(k) premarket notification submitted by Hangzhou AGS MedTech Co., Ltd. for the device "Sphincterotome". The FDA issued a decision of Substantially Equivalent on Feb 5, 2021. The device falls under product code KNS (Unit, Electrosurgical, Endoscopic (With Or Without Accessories)), a Class II device regulated under 21 CFR 876.4300. Hangzhou AGS MedTech Co., Ltd. has 18 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 5, 2021
- Date Received
- Apr 27, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
- Device Class
- Class II
- Regulation Number
- 876.4300
- Review Panel
- GU
- Submission Type
- 510(k)