Clearance Summary
ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1 received FDA 510(k) clearance under submission number K852309, sponsored by Erika, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1985-07-26.
- Submission: K852309
- Applicant / Sponsor: Erika, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1985-07-26
Classification & Regulation
This clearance is catalogued under FDA product code FJK and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.