Clearance Summary
CAPD PREP KIT received FDA 510(k) clearance under submission number K833780, sponsored by Professional Dialysis Products. 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 1984-02-09.
- Submission: K833780
- Applicant / Sponsor: Professional Dialysis Products
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5820
- Decision date: 1984-02-09
Classification & Regulation
This clearance is catalogued under FDA product code FKG and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class I device.