Virtual Imaging, Inc.
Virtual Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2010, with 2 FDA device recalls on record.
Top product codes for Virtual Imaging, Inc.
FDA recalls by Virtual Imaging, Inc.
- Z-0460-2019 — RadPRO(R) Mobile 40kW Digital X-Ray System - Model: SM-40HF-B-D-C Product Usage: Instrument is used to take diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric subjects. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. Not for mammography
- Z-1064-2015 — Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Virtual Imaging, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.