CHILLBUSTER— 510(k) K022903

Name: FDA 510(k) clearance K022903
Creator: U.S. Food and Drug Administration
Published: 2002-11-27

Substantially Equivalent

Microtek Medical, Inc.

FDA 510(k) clearance K022903 for CHILLBUSTER, Substantially Equivalent on 2002-11-27. Applicant: Microtek Medical, Inc.. Device class: 2.

Clearance details

Applicant: Microtek Medical, Inc.
Product code: Code DWJ
Device class: Class 2
Regulation: 21 CFR 870.5900
Advisory panel: Cardiovascular
Date received: 2002-09-03
Decision date: 2002-11-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, MS, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DWJ

product code DWJ

Death: 7
Injury: 679
Malfunction: 17,477
Total: 18,163

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.