Clearance Summary
MICROFUSE MEMBRANE INFUSION CATHETER received FDA 510(k) clearance under submission number K971619, sponsored by E-Med Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1998-02-27.
- Submission: K971619
- Applicant / Sponsor: E-Med Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1210
- Decision date: 1998-02-27
Classification & Regulation
This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.