Clearance Summary
ATLAS MONITOR, MODELS 200,210,220 received FDA 510(k) clearance under submission number K022084, sponsored by Welch Allyn, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-09-26.
- Submission: K022084
- Applicant / Sponsor: Welch Allyn, Inc.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2002-09-26
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.