Clearance Summary
VF-PD-120 received FDA 510(k) clearance under submission number K842460, sponsored by Valpey-Fisher Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1984-10-19.
- Submission: K842460
- Applicant / Sponsor: Valpey-Fisher Corp.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2880
- Decision date: 1984-10-19
Classification & Regulation
This clearance is catalogued under FDA product code JOP and 21 CFR 870.2880, within the Cardiovascular review panel as a Class II device.