CBYON SYSTEM WITH IMAGE ENHANCED FLUOROSCOPY MODULE— 510(k) K012886

Name: FDA 510(k) clearance K012886
Creator: U.S. Food and Drug Administration
Published: 2001-10-09

Substantially Equivalent

Cbyon, Inc.

FDA 510(k) clearance K012886 for CBYON SYSTEM WITH IMAGE ENHANCED FLUOROSCOPY MODULE, Substantially Equivalent on 2001-10-09. Applicant: Cbyon, Inc.. Device class: 2.

Clearance details

Applicant: Cbyon, Inc.
Product code: Code HAW
Device class: Class 2
Regulation: 21 CFR 882.4560
Advisory panel: Neurology
Date received: 2001-08-28
Decision date: 2001-10-09
Decision: Substantially Equivalent
Clearance type: Special
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HAW

product code HAW

Death: 52
Injury: 1,083
Malfunction: 17,300
Total: 18,435

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.