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SOYALA FULL FACE MASK

K061653 Class II Traditional
Decision Date
2006-11-09
Sponsor / Applicant
Weinmann Gerate Fur Medizin GmbH + Co. KG

Technical Specification

510(k) Submission ID K061653
Product Code BZD
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5905
Decision Date 2006-11-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOYALA FULL FACE MASK received FDA 510(k) clearance under submission number K061653, 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 2006-11-09.

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.