TRU-VIEW MULTI-CHANNEL DISPLAY— 510(k) K912008

Name: FDA 510(k) clearance K912008
Creator: U.S. Food and Drug Administration
Published: 1991-10-09

Substantially Equivalent

General Devices

FDA 510(k) clearance K912008 for TRU-VIEW MULTI-CHANNEL DISPLAY, Substantially Equivalent on 1991-10-09. Applicant: General Devices. Device class: 2.

Clearance details

Applicant: General Devices
Product code: Code DRT
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 1991-05-06
Decision date: 1991-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bogota, NJ, 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.