Clearance Summary
SOYALA GEL VENTED received FDA 510(k) clearance under submission number K081014, sponsored by Weinmann Gerate Fur Medizin GmbH + Co. KG. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2008-05-09.
- Submission: K081014
- Applicant / Sponsor: Weinmann Gerate Fur Medizin GmbH + Co. KG
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5905
- Decision date: 2008-05-09
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.