Clearance Summary
HERCULES 3 STAGE WIRE GUIDED DILATION BALLOON received FDA 510(k) clearance under submission number K090183, sponsored by Cook Endoscopy. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2009-09-25.
- Submission: K090183
- Applicant / Sponsor: Cook Endoscopy
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5365
- Decision date: 2009-09-25
Classification & Regulation
This clearance is catalogued under FDA product code KNQ and 21 CFR 876.5365, within the Gastroenterology, Urology review panel as a Class II device.