Clearance Summary
TREONIC C30 received FDA 510(k) clearance under submission number K840823, sponsored by Vickers America Medical Corp.. 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 1984-03-23.
- Submission: K840823
- Applicant / Sponsor: Vickers America Medical Corp.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5725
- Decision date: 1984-03-23
Classification & Regulation
This clearance is catalogued under FDA product code LDR and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.