Clearance Summary
MULTILINE; DLY-1 received FDA 510(k) clearance under submission number K930793, sponsored by Derma-Lase Co.. 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 1993-08-19.
- Submission: K930793
- Applicant / Sponsor: Derma-Lase Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 1993-08-19
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.