Clearance Summary
SOYALA, SOYALA BLUE received FDA 510(k) clearance under submission number K060405, sponsored by Weinmann Gerate Fur Medizin GmbH + Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2006-06-21.
- Submission: K060405
- Applicant / Sponsor: Weinmann Gerate Fur Medizin GmbH + Co. KG
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 2006-06-21
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.