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SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER

K913886 Class II Traditional
Decision Date
1992-01-24
Sponsor / Applicant
Sony Medical Electronics Co.

Technical Specification

510(k) Submission ID K913886
Product Code JAA
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1650
Decision Date 1992-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONY DVR-10 DIGITAL VIDEOCASSETTE RECORDER received FDA 510(k) clearance under submission number K913886, sponsored by Sony Medical Electronics Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code JAA and 21 CFR 892.1650, within the Radiology review panel as a Class II device.