Clearance Summary
HEM-O-LOK XL CLIP received FDA 510(k) clearance under submission number K030311, sponsored by Weck. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2003-02-26.
- Submission: K030311
- Applicant / Sponsor: Weck
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4300
- Decision date: 2003-02-26
Classification & Regulation
This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.