350 results · 31ms · Sources: EU EUDAMED, US FDA

IFA SENSIBAC STREPTOMYCIN

FDA 510(k)
FDA Class 2 ·Microbiology

ARiX RAD Radiographic System

FDA 510(k)
FDA Class 2 ·Radiology

IFA SENSIBAC CEFACLOR

FDA 510(k)
FDA Class 2 ·Microbiology

HEARTSCAN SOFTWARE

FDA 510(k)
FDA Class 2 ·Radiology

VAPOCIDE

FDA 510(k)
FDA Class 2 ·General Hospital

MARK IV FLOATATION THERAPY BED

FDA 510(k)
FDA Class 2 ·Physical Medicine

DOCTORS REVIEW SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Anti-Mutated Citrullinated Vimentin Igg

FDA classification
FDA Class 2 ·Anti-Mutated Citrullinated Vimentin Igg

AURORA SYSTEM 1000 SERIES HOME SELF-CARE SINGLE PATIENT DELIVERY SYSTEM; MODELS- SYS 1000, L3 WITH N100 ARM, 4B SOFTWARE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

BLOOD MONITOR PUMP WITH ULTRAFILTRATION CONTROLLER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX THREADED FUSION DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·VISTA LORDOTIC INTERBODY FUSION CAGE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BAK INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY TFC DEVICE/RAY TFC UNITE DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·RAY TFC UNITE PRODUCT LINE