Clearance Summary
INAMED RHEMO-D (TM) DILATOR received FDA 510(k) clearance under submission number K894618, sponsored by Inamed Development Co.. 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 1990-01-18.
- Submission: K894618
- Applicant / Sponsor: Inamed Development Co.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5450
- Decision date: 1990-01-18
Classification & Regulation
This clearance is catalogued under FDA product code FFP and 21 CFR 876.5450, within the Gastroenterology, Urology review panel as a Class I device.