Clearance Summary
KENDALL BLUNT TUOHY EPIDURAL NEEDLE received FDA 510(k) clearance under submission number K954706, sponsored by Kendall Healthcare Products Co. Div.Of Tyco Health. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1996-05-30.
- Submission: K954706
- Applicant / Sponsor: Kendall Healthcare Products Co. Div.Of Tyco Health
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5140
- Decision date: 1996-05-30
Classification & Regulation
This clearance is catalogued under FDA product code CAZ and 21 CFR 868.5140, within the Anesthesiology review panel as a Class II device.