Clearance Summary
COBE ACCESSORY INTERFACE MODULE (AIM) received FDA 510(k) clearance under submission number K861860, sponsored by Cobe Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-07-18.
- Submission: K861860
- Applicant / Sponsor: Cobe Laboratories, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.4205
- Decision date: 1986-07-18
Classification & Regulation
This clearance is catalogued under FDA product code KRL and 21 CFR 870.4205, within the Cardiovascular review panel as a Class II device.