Clearance Summary
MITRAL VALVE ORIFICE SIZER received FDA 510(k) clearance under submission number K820887, sponsored by Celtech. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1982-07-08.
- Submission: K820887
- Applicant / Sponsor: Celtech
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class I
- Regulation citation: 21 CFR 870.3945
- Decision date: 1982-07-08
Classification & Regulation
This clearance is catalogued under FDA product code DTI and 21 CFR 870.3945, within the Cardiovascular review panel as a Class I device.