SONY CINE VIDEO SYSTEM SME-3500— 510(k) K904447

Substantially Equivalent

Sony Medical Electronics Co.

FDA 510(k) clearance K904447 for SONY CINE VIDEO SYSTEM SME-3500, Substantially Equivalent on 1990-10-17. Applicant: Sony Medical Electronics Co..

Clearance details

Applicant
Sony Medical Electronics Co.
Product code
Code IZI
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Park Ridge, NJ, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code IZI

product code IZI
Death
9
Malfunction
5,312
Total
5,321

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.