Clearance Summary
SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD received FDA 510(k) clearance under submission number K885042, sponsored by Sony Medical Electronics Co.. 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 1988-12-22.
- Submission: K885042
- Applicant / Sponsor: Sony Medical Electronics Co.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4160
- Decision date: 1988-12-22
Classification & Regulation
This clearance is catalogued under FDA product code KQM and 21 CFR 878.4160, within the General, Plastic Surgery review panel as a Class I device.