Clearance Summary
LDV((Low Dead Volume )Syringe received FDA 510(k) clearance under submission number K220083, sponsored by Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.. 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 2022-05-25.
- Submission: K220083
- Applicant / Sponsor: Anhui Hongyu Wuzhou Medical Manufacturer Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5860
- Decision date: 2022-05-25
Classification & Regulation
This clearance is catalogued under FDA product code QNQ and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.