Clearance Summary
VITALERT 3000 MONITORING SYSTEM received FDA 510(k) clearance under submission number K913995, sponsored by Draeger Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1992-11-03.
- Submission: K913995
- Applicant / Sponsor: Draeger Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.1400
- Decision date: 1992-11-03
Classification & Regulation
This clearance is catalogued under FDA product code CCK and 21 CFR 868.1400, within the Anesthesiology review panel as a Class II device.