Clearance Summary
DISPOS. & SPONGE FORCEPS PEAN ARTERY received FDA 510(k) clearance under submission number K843074, sponsored by Greene International Corp.. 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 1984-08-17.
- Submission: K843074
- Applicant / Sponsor: Greene International Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1984-08-17
Classification & Regulation
This clearance is catalogued under FDA product code GEN and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.