Clearance Summary
CUFF SPECULUM received FDA 510(k) clearance under submission number K893531, sponsored by Mountain Medical Equipment, 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 1989-06-22.
- Submission: K893531
- Applicant / Sponsor: Mountain Medical Equipment, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5220
- Decision date: 1989-06-22
Classification & Regulation
This clearance is catalogued under FDA product code KPL and 21 CFR 876.5220, within the Gastroenterology, Urology review panel as a Class II device.