Clearance Summary
ES Series V2 received FDA 510(k) clearance under submission number K232336, sponsored by E-Scopics. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-09-26.
- Submission: K232336
- Applicant / Sponsor: E-Scopics
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2023-09-26
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.