Clearance Summary
SONY LASER VIDEODISC RECORDING SYSTEM received FDA 510(k) clearance under submission number K921275, sponsored by Sony Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-06-10.
- Submission: K921275
- Applicant / Sponsor: Sony Medical Systems
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.2010
- Decision date: 1992-06-10
Classification & Regulation
This clearance is catalogued under FDA product code LMB and 21 CFR 892.2010, within the Radiology review panel as a Class I device.