TWLIGHT, MODEL ISP 9600— 510(k) K022642

Substantially Equivalent

Invacare Corp.

FDA 510(k) clearance K022642 for TWLIGHT, MODEL ISP 9600, Substantially Equivalent on 2003-02-11. Applicant: Invacare Corp..

Clearance details

Applicant: Invacare Corp.
Product code: Code BZD
Advisory panel: Anesthesiology
Date received: 2002-08-08
Decision date: 2003-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elyria, OH, US

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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.