Clearance Summary
SINGLE-PATIENT AUTOMATIC DIALYSIS UNIT MOD. DBB-22 received FDA 510(k) clearance under submission number K863609, sponsored by International Medical Products, 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 1987-02-25.
- Submission: K863609
- Applicant / Sponsor: International Medical Products, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1987-02-25
Classification & Regulation
This clearance is catalogued under FDA product code FKP and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.