Clearance Summary
Sterile Auto-Disable Syringes with/without Needle for Single Use received FDA 510(k) clearance under submission number K211210, sponsored by Azur Medical Company, 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 2022-01-27.
- Submission: K211210
- Applicant / Sponsor: Azur Medical Company, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2022-01-27
Classification & Regulation
This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.