Clearance Summary
DMS 3000 received FDA 510(k) clearance under submission number K792252, sponsored by Renal Care Corp.. 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 1980-03-12.
- Submission: K792252
- Applicant / Sponsor: Renal Care Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1980-03-12
Classification & Regulation
This clearance is catalogued under FDA product code FKQ and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.