SC1 Handheld Ultrasound Imaging system (Model: SC1)— 510(k) K233579

Substantially Equivalent

Fcu Co., Ltd.

FDA 510(k) clearance K233579 for SC1 Handheld Ultrasound Imaging system (Model: SC1), Substantially Equivalent on 2024-06-26. Applicant: Fcu Co., Ltd..

Clearance details

Applicant: Fcu Co., Ltd.
Product code: Code IYO
Advisory panel: Radiology
Date received: 2023-11-07
Decision date: 2024-06-26
Decision: Substantially Equivalent
Clearance type: Special
Location: Yuseong-Gu, KR

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.