Clearance Summary
CURITY FAST-CATH FEMALE CATHETER KIT received FDA 510(k) clearance under submission number K935774, sponsored by Kendall Healthcare Products Co. Div.Of Tyco Health. 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 1994-04-11.
- Submission: K935774
- Applicant / Sponsor: Kendall Healthcare Products Co. Div.Of Tyco Health
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class I
- Regulation citation: 21 CFR 876.5250
- Decision date: 1994-04-11
Classification & Regulation
This clearance is catalogued under FDA product code EYT and 21 CFR 876.5250, within the Gastroenterology, Urology review panel as a Class I device.