CTC WORKSTATION, MODEL 2200— 510(k) K062229

Name: FDA 510(k) clearance K062229
Creator: U.S. Food and Drug Administration
Published: 2006-09-11

Substantially Equivalent

Medical Diagnostic Technologies, Inc.

FDA 510(k) clearance K062229 for CTC WORKSTATION, MODEL 2200, Substantially Equivalent on 2006-09-11. Applicant: Medical Diagnostic Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Medical Diagnostic Technologies, Inc.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2006-08-02
Decision date: 2006-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Las Vegas, NV, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.