NUWAV— 510(k) K081781

Substantially Equivalent

Laborie Medical Technologies, Corp.

FDA 510(k) clearance K081781 for NUWAV, Substantially Equivalent on 2008-07-09. Applicant: Laborie Medical Technologies, Corp..

Clearance details

Applicant: Laborie Medical Technologies, Corp.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2008-06-24
Decision date: 2008-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Williston, VT, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.