Clearance Summary
REMOVE ADHESIVE REMOVER received FDA 510(k) clearance under submission number K893603, sponsored by Smith & Nephew United, 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 1989-07-14.
- Submission: K893603
- Applicant / Sponsor: Smith & Nephew United, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4730
- Decision date: 1989-07-14
Classification & Regulation
This clearance is catalogued under FDA product code KOX and 21 CFR 878.4730, within the General, Plastic Surgery review panel as a Class I device.