Clearance Summary
MEDLEY SP02 MODULE, MODEL 8220 received FDA 510(k) clearance under submission number K010966, sponsored by Alaris Medical Systems, 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 2001-06-08.
- Submission: K010966
- Applicant / Sponsor: Alaris Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2001-06-08
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.