Clearance Summary
3-WAY STOPCOCK WITH LUER-LOCK FITTING received FDA 510(k) clearance under submission number K770154, sponsored by American Viggo. 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 1977-02-28.
- Submission: K770154
- Applicant / Sponsor: American Viggo
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4200
- Decision date: 1977-02-28
Classification & Regulation
This clearance is catalogued under FDA product code KGZ and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.