FUJIFILM FC1 Ultrasound System— 510(k) K160406

Substantially Equivalent

FUJIFILM Sonosite, Inc.

FDA 510(k) clearance K160406 for FUJIFILM FC1 Ultrasound System, Substantially Equivalent on 2016-03-16. Applicant: FUJIFILM Sonosite, Inc..

Clearance details

Applicant: FUJIFILM Sonosite, Inc.
Product code: Code IYN
Advisory panel: Radiology
Date received: 2016-02-16
Decision date: 2016-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bothell, WA, US

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Adverse events under product code IYN

product code IYN

Death: 25
Injury: 163
Malfunction: 1,538
Other: 4
Total: 1,730

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.