Clearance Summary
DEBUTRON received FDA 510(k) clearance under submission number K782119, sponsored by Martin Electric Co.. 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 1979-02-26.
- Submission: K782119
- Applicant / Sponsor: Martin Electric Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.5360
- Decision date: 1979-02-26
Classification & Regulation
This clearance is catalogued under FDA product code KCX and 21 CFR 878.5360, within the General, Plastic Surgery review panel as a Class I device.