Clearance Summary
HAND-HELD RETRACTOR, DISSECTOR & DISSECTOR received FDA 510(k) clearance under submission number K955120, sponsored by Ethicon Endo-Surgery, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1996-01-26.
- Submission: K955120
- Applicant / Sponsor: Ethicon Endo-Surgery, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1996-01-26
Classification & Regulation
This clearance is catalogued under FDA product code GCM and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.