Clearance Summary
DISPOSABLE CAUTERY ABRASIVE PAD received FDA 510(k) clearance under submission number K915064, sponsored by American Medical Mfg., 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 1992-03-11.
- Submission: K915064
- Applicant / Sponsor: American Medical Mfg., Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1992-03-11
Classification & Regulation
This clearance is catalogued under FDA product code KDC and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.