PRESCOTT'S LIGHT SOURCE MODEL NO. II-150

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Estacore-Pro Automatic Biopsy Needle, Geotek Semiautomatic Biopsy Needle, Maxicore-M Automatic Biopsy Gun Needle, Maxicore-M Automatic Biopsy Needle and Instrument

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

GTK Disposable Needle Guides

FDA 510(k)

FDA Class 2 ·Radiology

myQA iON

FDA 510(k)

FDA Class 2 ·Radiology

Blue Phantom PT

FDA 510(k)

FDA Class 2 ·Radiology

OMNIPRO INCLINE

FDA 510(k)

FDA Class 2 ·Radiology

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·SCIMED PTCA CATHETERS

IBA PROTON THERAPY SYSTEM, PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

IBA PROTON THERAPY SYSTEM - PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

IBA PROTON THERAPY SYSTEM-PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

IBA PROTON THERAPY SYSTEM - PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

IBA PROTON THERAPY SYSTEM- PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

IBA PROTON THERAPY SYSTEM - PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

Tissue Adhesive For The Topical Approximation Of Skin

FDA Pre-Market Approval

FDA Class 2 ·DERMABOND TOPICAL SKIN ADHESIVE

IBA PROTON THERAPY SYSTEM, MODEL PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

MODIFICATION TO IBA PROTON THERAPY SYSTEM-PROTEUS 235

FDA 510(k)

FDA Class 2 ·Radiology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·INTER FIX THREADED FUSION DEVICE, INTER FIX RP THREADED FUSION DEVICE AND LT-CAGE LUMBAR TAPERED FUSION DEVICE

IBA Proton Therapy System- Proteus 235 (Proteus One, Proteus Plus, Proteus TK2, Proteus Class)

FDA 510(k)

FDA Class 2 ·Radiology

NM-01/CPT neurometer (NM-01/CPT)

FDA 510(k)

FDA Class 2 ·Neurology