Clearance Summary
MEDISYSTEMS PHERESIS NEEDLE received FDA 510(k) clearance under submission number K862002, sponsored by Medisystems 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 1986-06-27.
- Submission: K862002
- Applicant / Sponsor: Medisystems Corp.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 1986-06-27
Classification & Regulation
This clearance is catalogued under FDA product code FIE and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.