Clearance Summary
SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE received FDA 510(k) clearance under submission number K970837, sponsored by Somnus Medical Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1998-01-09.
- Submission: K970837
- Applicant / Sponsor: Somnus Medical Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 1998-01-09
Classification & Regulation
This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.