Clearance Summary
VITAJET JET INSULIN INJECTION DEVICE received FDA 510(k) clearance under submission number K843784, sponsored by Vitajet Industriae Comercioltda.. 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 1984-11-02.
- Submission: K843784
- Applicant / Sponsor: Vitajet Industriae Comercioltda.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5430
- Decision date: 1984-11-02
Classification & Regulation
This clearance is catalogued under FDA product code KZE and 21 CFR 880.5430, within the General Hospital review panel as a Class II device.