520 DISPLAY DRIVER- STATUS I— 510(k) K926298

Name: FDA 510(k) clearance K926298
Creator: U.S. Food and Drug Administration
Published: 1994-05-04

Substantially Equivalent

Vidco, Inc.

FDA 510(k) clearance K926298 for 520 DISPLAY DRIVER- STATUS I, Substantially Equivalent on 1994-05-04. Applicant: Vidco, Inc.. Device class: 2.

Clearance details

Applicant: Vidco, Inc.
Product code: Code DRT
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 1992-12-14
Decision date: 1994-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beaverton, OR, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DRT

product code DRT

Death: 4
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.