Clearance Summary
REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY received FDA 510(k) clearance under submission number K930666, sponsored by Snowden-Pencer. 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 1994-05-19.
- Submission: K930666
- Applicant / Sponsor: Snowden-Pencer
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 1994-05-19
Classification & Regulation
This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.