Clearance Summary
NEEDLE/CANNULA received FDA 510(k) clearance under submission number K950574, sponsored by Tri-Med Specialties, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1995-02-24.
- Submission: K950574
- Applicant / Sponsor: Tri-Med Specialties, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4370
- Decision date: 1995-02-24
Classification & Regulation
This clearance is catalogued under FDA product code LRO and 21 CFR 878.4370, within the General, Plastic Surgery review panel as a Class II device.