Clearance Summary
GRASPING FORCEP (W/FOUR PRONGS) received FDA 510(k) clearance under submission number K792100, sponsored by Eder Instrument Co, 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 1979-11-13.
- Submission: K792100
- Applicant / Sponsor: Eder Instrument Co, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1979-11-13
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.