Clearance Summary
TRACE MODEL #'S 840, 841, 842, 845 received FDA 510(k) clearance under submission number K925145, sponsored by Trace Medical Equipment, 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 1993-05-19.
- Submission: K925145
- Applicant / Sponsor: Trace Medical Equipment, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.3910
- Decision date: 1993-05-19
Classification & Regulation
This clearance is catalogued under FDA product code FYH and 21 CFR 878.3910, within the General, Plastic Surgery review panel as a Class I device.