Clearance Summary
S3086 ARTERIAL, S3087 VENOUS NEONATAL HEMODIALYSIS received FDA 510(k) clearance under submission number K873455, sponsored by Dravon Medical, 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 1987-09-14.
- Submission: K873455
- Applicant / Sponsor: Dravon Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5820
- Decision date: 1987-09-14
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.