NDOHD HIGH DEFINITION IMAGING SYSTEM (NDOHD)— 510(k) K131873

Substantially Equivalent

MethodSense, Inc.

FDA 510(k) clearance K131873 for NDOHD HIGH DEFINITION IMAGING SYSTEM (NDOHD), Substantially Equivalent on 2013-09-25. Applicant: MethodSense, Inc..

Clearance details

Applicant: MethodSense, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2013-06-24
Decision date: 2013-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Durham, NC, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.