Clearance Summary
AIMED DISPOS. INJECTION NEEDLE received FDA 510(k) clearance under submission number K842230, sponsored by Tech-Cons Ltd., Intl.. 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 1984-08-17.
- Submission: K842230
- Applicant / Sponsor: Tech-Cons Ltd., Intl.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1984-08-17
Classification & Regulation
This clearance is catalogued under FDA product code GAA and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.