PURTIAN BENNETT, GOOD KNIGHT 420G MODEL M-113900-US; PURTAN BENNETT, GOODKNIGHT 420S MODEL M-113903-US— 510(k) K020886

Name: FDA 510(k) clearance K020886
Creator: U.S. Food and Drug Administration
Published: 2002-11-01

Substantially Equivalent

Tyco Healthcare Nancy

FDA 510(k) clearance K020886 for PURTIAN BENNETT, GOOD KNIGHT 420G MODEL M-113900-US; PURTAN BENNETT, GOODKNIGHT 420S MODEL M-113903-US, Substantially Equivalent on 2002-11-01. Applicant: Tyco Healthcare Nancy. Device class: 2.

Clearance details

Applicant: Tyco Healthcare Nancy
Product code: Code BZD
Device class: Class 2
Regulation: 21 CFR 868.5905
Advisory panel: Anesthesiology
Date received: 2002-03-18
Decision date: 2002-11-01
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Villers-Les-Nancy Cedex, FR

Download summary PDF View on FDA.gov ↗

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Adverse events under product code BZD

product code BZD

Death: 4,440
Injury: 53,099
Malfunction: 213,222
Other: 17
Total: 270,778

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.