Clearance Summary
SWIVEL ELBOW received FDA 510(k) clearance under submission number K000215, sponsored by Engineered Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2000-05-26.
- Submission: K000215
- Applicant / Sponsor: Engineered Medical Systems
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 2000-05-26
Classification & Regulation
This clearance is catalogued under FDA product code BZD and 21 CFR 868.5905, within the Anesthesiology review panel as a Class II device.