Clearance Summary
MED-LOK SAFETY NEEDLE received FDA 510(k) clearance under submission number K103781, sponsored by Sta-Med, LLC. 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 2011-02-08.
- Submission: K103781
- Applicant / Sponsor: Sta-Med, LLC
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2011-02-08
Classification & Regulation
This clearance is catalogued under FDA product code MEG and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.