Clearance Summary
29G AND 30G K-PACK II NEEDLE received FDA 510(k) clearance under submission number K062608, sponsored by Terumo Europe N.V.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2006-09-15.
- Submission: K062608
- Applicant / Sponsor: Terumo Europe N.V.
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 2006-09-15
Classification & Regulation
This clearance is catalogued under FDA product code FMI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.