Clearance Summary
INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KIT received FDA 510(k) clearance under submission number K932692, sponsored by Innerdyne Medical, 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 1993-12-27.
- Submission: K932692
- Applicant / Sponsor: Innerdyne Medical, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1993-12-27
Classification & Regulation
This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.