Clearance Summary
MODIFICATION TO TEMNO BIOPSY NEEDLES received FDA 510(k) clearance under submission number K024120, sponsored by Allegiance Healthcare Corp.. 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 2003-01-15.
- Submission: K024120
- Applicant / Sponsor: Allegiance Healthcare Corp.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1075
- Decision date: 2003-01-15
Classification & Regulation
This clearance is catalogued under FDA product code FCG and 21 CFR 876.1075, within the Gastroenterology, Urology review panel as a Class II device.