Clearance Summary
NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER received FDA 510(k) clearance under submission number K910890, sponsored by Lovell-Schenck, 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 1991-06-27.
- Submission: K910890
- Applicant / Sponsor: Lovell-Schenck, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4040
- Decision date: 1991-06-27
Classification & Regulation
This clearance is catalogued under FDA product code LYU and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class I device.