Clearance Summary
TERUMO DISPOSABLE SPINAL NEEDLE received FDA 510(k) clearance under submission number K760775, sponsored by Terumo America, 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 1976-11-01.
- Submission: K760775
- Applicant / Sponsor: Terumo America, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1976-11-01
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.