Clearance Summary
SMITH & NEPHEW SUBCUTANEOUS ILLUMINATOR received FDA 510(k) clearance under submission number K991323, sponsored by Smith & Nephew, 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 1999-07-06.
- Submission: K991323
- Applicant / Sponsor: Smith & Nephew, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1999-07-06
Classification & Regulation
This clearance is catalogued under FDA product code FFS and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.