Clearance Summary
Promisemed Safety Huber Needle received FDA 510(k) clearance under submission number K230715, sponsored by Promisemed Hangzhou Meditech 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 2023-06-08.
- Submission: K230715
- Applicant / Sponsor: Promisemed Hangzhou Meditech Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5570
- Decision date: 2023-06-08
Classification & Regulation
This clearance is catalogued under FDA product code PTI and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.