Lumbar IBFD

FDA UDI

KEOS·B084KPS12308100·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308080·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308130·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308150·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308140·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308060·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308110·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308120·

Lumbar IBFD

FDA UDI

KEOS·B084KPS12308090·

STRATUS CS D-DIMER

FDA 510(k)

FDA Class 2 ·Hematology

DADE THROMBIN REAGENT

FDA 510(k)

FDA Class 2 ·Hematology

DIMENSION URINE ECSTASY SCREEN FLEX REAGENT CARTRIDGE, MODEL DF 109

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

N ANTISERA TO HUMAN COMPLEMENT FACTORS (C3C, C4)

FDA 510(k)

FDA Class 2 ·Immunology

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MODEL 2920 PRM SYSTEM ZOOM (VENTAK PRX AICD SYSTEM)

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX & VENTAK MINI ICD: LATTITUDE PATIENT MANAGMENT SYSTEM

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AND VENTAK MINI AUTOMATED IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ACID) SYSTEMS

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AICD SYSTEM. PRESCRIPTOR PROGRAMMER AND PROGRAM AND PROGRAM DISK

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AND VENTAK MINI AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (AICD) FAMILIES

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·VENTAK PRX AND VENTAK MINI AUTOMATIC IMPLANTABLE CARDIOVERSTER DEFIBRILLATOR (AICD) FAMILIES

Artemis Hand Held Imaging System

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology