Clearance Summary
ASAHI AM-BIO SERIES DIALYZERS (WET MODELS)& (DRY MODELS), MODELS AM-BIO-50,AM-BIO-65, AM-BIO-75, AND AM-BIO-100, AM-BIO- received FDA 510(k) clearance under submission number K983720, sponsored by Asahi Medical Co., Ltd.. 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 1999-05-17.
- Submission: K983720
- Applicant / Sponsor: Asahi Medical Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1999-05-17
Classification & Regulation
This clearance is catalogued under FDA product code MSE and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.