510(k) K241285
K241285 is an FDA 510(k) premarket notification submitted by Alton (Shanghai) Medical Instruments Co., Ltd. for the device "Disposable Endoscope Valves Set (AF series)". The FDA issued a decision of Substantially Equivalent on October 1, 2024. The device falls under product code ODC (Endoscope Channel Accessory), a Class II device regulated under 21 CFR 876.1500. Alton (Shanghai) Medical Instruments Co., Ltd. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 1, 2024
- Date Received
- May 7, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoscope Channel Accessory
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- GU
- Submission Type
To give the endoscope channel additional or improved functionality.