TERRAQUANT MQ2000 LASER THERAPY DEVICE— 510(k) K043055

Substantially Equivalent

Escada International, Inc.

FDA 510(k) clearance K043055 for TERRAQUANT MQ2000 LASER THERAPY DEVICE, Substantially Equivalent on 2005-07-25. Applicant: Escada International, Inc..

Clearance details

Applicant: Escada International, Inc.
Product code: Code ILY
Advisory panel: Physical Medicine
Date received: 2004-11-05
Decision date: 2005-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

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Adverse events under product code ILY

product code ILY

Death: 3
Total: 3

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.