Ziehm Imaging, Inc.
Ziehm Imaging, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2009, with 14 FDA device recalls on record.
Top product codes for Ziehm Imaging, Inc.
FDA recalls by Ziehm Imaging, Inc.
10 most recent of 14- Z-1893-2017 — Ziehm Imaging solo FD Mobile Fluoroscopic C-arm
- Z-2643-2016 — Ziehm Solo, Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-2642-2016 — Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-2644-2016 — Ziehm Vision2, Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-2641-2016 — Ziehm Vision RFD, Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-2640-2016 — Ziehm Vision RFD Mot, Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-2639-2016 — Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging
- Z-0563-2014 — Ziehm Solo C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
- Z-0568-2014 — Ziehm Vision RFD C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
- Z-0565-2014 — Ziehm Vision(2) C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
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 Ziehm Imaging, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.