Clearance Summary
RETRAX RETRACTING NEEDLE SYRINGE, SIZE 3CC received FDA 510(k) clearance under submission number K001017, sponsored by Retrax Safety Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2000-06-02.
- Submission: K001017
- Applicant / Sponsor: Retrax Safety Systems, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2000-06-02
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.