NAVITRACK SYSTEM-OS KNEE UNIVERSAL, MODEL PRO-05002

FDA 510(k)

FDA Class 2 ·Neurology

ROSA Knee System

FDA 510(k)

FDA Class 2 ·Neurology

IASSIST KNEE SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

NAVITRACK SYSTEM-OPTICAL TKR CT-LESS, MODEL 900.120

FDA 510(k)

FDA Class 2 ·Neurology

EPTFE SHEET COVERING FOR OCULAR IMPLANT

FDA 510(k)

FDA Class 2 ·Ophthalmic

ROSA® Knee System

FDA 510(k)

FDA Class 2 ·Neurology

Ventway Sparrow

FDA 510(k)

FDA Class 2 ·Anesthesiology

Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment

FDA classification

FDA Class 2 ·Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment

Rongeur, Cystoscopic, Hot

FDA classification

FDA Class 2 ·Rongeur, Cystoscopic, Hot

Device, Pasteurization, Hot Water

FDA classification

FDA Class 2 ·Device, Pasteurization, Hot Water

Bag, Urine Collection, Newborn

FDA classification

FDA Class 2 ·Bag, Urine Collection, Newborn

Pack, Hot Or Cold, Water Circulating

FDA classification

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

Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma

FDA classification

FDA Class 2 ·Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma

Tenaculum, Uterine, Exempt

FDA classification

FDA Class 2 ·Tenaculum, Uterine, Exempt

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)