Clearance Summary
THE S. CORDERO STYLUS received FDA 510(k) clearance under submission number K863808, sponsored by S. Cordero 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 1986-10-14.
- Submission: K863808
- Applicant / Sponsor: S. Cordero Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1986-10-14
Classification & Regulation
This clearance is catalogued under FDA product code GDZ and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.