Scanmate Flex— 510(k) K171301

Substantially Equivalent

Dgh Technology, Inc.

FDA 510(k) clearance K171301 for Scanmate Flex, Substantially Equivalent on 2017-07-31. Applicant: Dgh Technology, Inc..

Clearance details

Applicant: Dgh Technology, Inc.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2017-05-03
Decision date: 2017-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Exton, PA, 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.