Medical Device Manufacturer · US , Owings Mills , MD

I.Z.I. Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1992

7

Total

7

Cleared

0

Denied

I.Z.I. Corp. has 7 FDA 510(k) cleared medical devices. Based in Owings Mills, US.

Historical record: 7 cleared submissions from 1992 to 2002. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by I.Z.I. Corp. Filter by specialty or product code using the sidebar.

7 devices

1–7 of 7

K022074 · HAW Neurological Stereotaxic Instrument · Neurology

MRI LINE MARKER

K014022 · IYE Accelerator, Linear, Medical · Radiology

MRI LINE MARKER

K003736 · JAK System, X-ray, Tomography, Computed · Radiology

K994117 · LNH System, Nuclear Magnetic Resonance Imaging · Radiology

K993742 · IYE Accelerator, Linear, Medical · Radiology

CT/MRI TOPOGRAPHIC MARKER

K930752 · JAC System, X-ray, Film Marking, Radiographic · Radiology

E.Z. PORT(TM) RADIATION THERAPY SKIN MARKERS

K922287 · KPQ System, Simulation, Radiation Therapy · Radiology