CEREBASE DA Guide Sheath, 95cm, CEREBASE DA Guide Sheath, 90cm, CEREBASE DA Guide Sheath, 80cm, CEREBASE DA Guide Sheath, 70cm

FDA 510(k)

FDA Class 2 ·Cardiovascular

PLASMA EDGE System

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Omnimax S3, Omnimax S4

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

CARD GUARD, MODEL CG-7100

FDA 510(k)

FDA Class 2 ·Cardiovascular

MCB UNIT Model: V10GMCBUS

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

TRUESPAN Meniscal Repair System

FDA 510(k)

FDA Class 2 ·Orthopedic

FMS VUE II Fluid Management and Tissue Debridement System

FDA 510(k)

FDA Class 2 ·Orthopedic

Rapid Family

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

PERMATAPE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

PETERIO UNIVERSAL LASER SCANNING HANDPIECE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

VX120 Ophthalmic Diagnostic Device

FDA 510(k)

FDA Class 2 ·Ophthalmic

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

FDA Pre-Market Approval

FDA Class 2 ·Dimension Vista TPSA Flex reagent cartridge (K6451)

Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

FDA Pre-Market Approval

FDA Class 2 ·IMMULITE 2500 PSA, IMMULITE 2500 THIRD GENERATION PSA

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·RAY TFC UNITE PRODUCT LINE

Cytomegalovirus (Cmv) Dna Quantitative Assay

FDA Pre-Market Approval

FDA Class 2 ·Alinity m CMV

Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus

FDA Pre-Market Approval

FDA Class 2 ·Alinity m HCV

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

Catheters, Transluminal Coronary Angioplasty, Percutaneous

FDA Pre-Market Approval

FDA Class 2 ·MAVERICK XL PTCA CATHETER (MONORAIL)

Computer, Diagnostic, Pre-Programmed, Single-Function

FDA classification

FDA Class 2 ·Computer, Diagnostic, Pre-Programmed, Single-Function

Cement, Bone, Vertebroplasty, Pre-Formed, Modular

FDA classification

FDA Class 2 ·Cement, Bone, Vertebroplasty, Pre-Formed, Modular