F3— 510(k) K222998

Substantially Equivalent

Acrew Imaging, Inc.

FDA 510(k) clearance K222998 for F3, Substantially Equivalent on 2023-06-20. Applicant: Acrew Imaging, Inc..

Clearance details

Applicant: Acrew Imaging, Inc.
Product code: Code OWB
Advisory panel: Radiology
Date received: 2022-09-28
Decision date: 2023-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ocean View, DE, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code OWB

product code OWB

Death: 49
Injury: 340
Malfunction: 36,973
Total: 37,362

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.