GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71; GIMMI ALPHA BRONCHOSCOPES MODEL # E.8189.00/01/02/03

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Ventway Sparrow

FDA 510(k)

FDA Class 2 ·Anesthesiology

Normalizing Quantitative Electroencephalograph Software

FDA classification

FDA Class 2 ·Normalizing Quantitative Electroencephalograph Software

Rongeur, Cystoscopic, Hot

FDA classification

FDA Class 2 ·Rongeur, Cystoscopic, Hot

Device, Pasteurization, Hot Water

FDA classification

FDA Class 2 ·Device, Pasteurization, Hot Water

Bronchoscope (Flexible Or Rigid)

FDA classification

FDA Class 2 ·Bronchoscope (Flexible Or Rigid)

Pack, Hot Or Cold, Water Circulating

FDA classification

FDA Class 2 ·Pack, Hot Or Cold, Water Circulating

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·THE NEEDLE DESTROYER

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·THE DISINTEGRATOR PLUS LANCE/INSULIN NEEDLE DESTRUCTON DEVICE

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·THE DISINTEGRATOR INSULIN NEEDLE DESTRUCTION DEVICE

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·SHARP(X)TM NEEDLE DESTRUCTION UNIT

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·SHARP NEEDLE DESTRUCTION UNIT

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NEEDLE ZAP (R)

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NEEDLE ZAP

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·SHARPX NEEDLE DESTRUCTION UNIT

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·THE NEEDLYZER - THE NEEDLE DESTROYER MODEL ND2

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NIC 1800 NEEDLE DISPOSAL SYSTEM

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·Sharps Terminator

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·Q 103 NEEDLE MANAGEMENT SYSTEM

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NEEDLE-EASE TM 2501