Clearance Summary
SURGICAL PREP RAZOR received FDA 510(k) clearance under submission number K874370, sponsored by Derma-Safe 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 1987-11-13.
- Submission: K874370
- Applicant / Sponsor: Derma-Safe Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1987-11-13
Classification & Regulation
This clearance is catalogued under FDA product code LWK and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.