Clearance Summary
SEPP ADHESIVE REMOVER received FDA 510(k) clearance under submission number K934790, sponsored by Medi-Flex Hospital Products, 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 1994-03-11.
- Submission: K934790
- Applicant / Sponsor: Medi-Flex Hospital Products, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4730
- Decision date: 1994-03-11
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.