BIS EEG VISTA MONITOR SYSTEM AND BISX

FDA 510(k)

FDA Class 2 ·Neurology

360 DEG. ROTATING 1/2 BEAM BLOCK

FDA 510(k)

FDA Class 2 ·Radiology

PRECISION EEG CAP W/ELECTRODE SET AND

FDA 510(k)

FDA Class 2 ·Neurology

PANBUS DIGITAL EEG & SLEEP ACQUISITION DEVICES

FDA 510(k)

FDA Class 2 ·Neurology

BUNNY ELECTRODE/STEALTH ELECTRODE PRE WIRED EEG

FDA 510(k)

FDA Class 2 ·Cardiovascular

EEG MONITOR WITH BIS, MODEL A-2000

FDA 510(k)

FDA Class 2 ·Neurology

Persyst 15 EEG Review and Analysis Software

FDA 510(k)

FDA Class 2 ·Neurology

NIHON KOHDEN QP-160AK EEG TREND PROGRAM

FDA 510(k)

FDA Class 2 ·Neurology

EMG SURFACE, DIGITAL RING, BAR, GROUNDING, EEG

FDA 510(k)

FDA Class 2 ·Neurology

Nihon Kohden QP-160AK EEG Trend Program

FDA 510(k)

FDA Class 2 ·Neurology

PERSYST 12 EEG REVIEW AND ANALYSIS SOFTWARE

FDA 510(k)

FDA Class 2 ·Neurology

MODEL 4000 EEG MONITOR WITH PSI (PSA4000)

FDA 510(k)

FDA Class 2 ·Neurology

Persyst 14 EEG Review and Analysis Software

FDA 510(k)

FDA Class 2 ·Neurology

Amydi-med Disposable Non-invasive EEG electrodes

FDA 510(k)

FDA Class 2 ·Neurology

WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WITHOUT, PULSE OXIMETRY,CARDINAL DIGITAL EEG AND SLEEP ACQUIS

FDA 510(k)

FDA Class 2 ·Neurology

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval

FDA Class 2 ·GEN-PROBE AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST(MTD TEST)

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval

FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval

FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval

FDA Class 2 ·GEN-PROBE(R) AMPLIFIED MYCOBACTERIUM TUBERCULOSIS DIRECT TEST (MTD TEST)

System, Nucleic Acid Amplification, Mycobacterium Tuberculosis Complex

FDA Pre-Market Approval

FDA Class 2 ·AMPLIFIED MTD (MYCOBACTERIUM TUBERCULOSIS DIRECT) TEST