4,373 results · 35ms · Sources: EU EUDAMED, US FDA

Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN Disposable Concentric Needle Electrodes-37mm, Dantec DCN Disposable Concentric Needle Electrodes-50mm, Dantec DCN Disposable Concentric Needle Electrodes-75mm

FDA 510(k)
FDA Class 2 ·Physical Medicine

MYOVISION 3.0 WIREFREE SYSTEM

FDA 510(k)
FDA Class 2 ·Physical Medicine

Hair Boom 69

FDA 510(k)
FDA Class 2 ·Physical Medicine

Hair Growth Device

FDA 510(k)
FDA Class 2 ·Physical Medicine

BIOPAK MEASUREMENT SYSTEM

FDA 510(k)
FDA Class 2 ·Physical Medicine

RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP

FDA 510(k)
FDA Class 2 ·Physical Medicine

Assay, Proliferation, In Vitro, T Lymphocyte

FDA classification
FDA Class 2 ·Assay, Proliferation, In Vitro, T Lymphocyte

Gastrointestinal Capsule Endoscopy Analysis Software Device

FDA classification
FDA Class 2 ·Gastrointestinal Capsule Endoscopy Analysis Software Device

System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection

FDA classification
FDA Class 2 ·System, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Mutation Detection

Table Mounted Miniaturized Electromechanical Surgical System

FDA classification
FDA Class 2 ·Table Mounted Miniaturized Electromechanical Surgical System

System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection

FDA classification
FDA Class 2 ·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Mutations & Variants Panel Sequencing Detection

System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection

FDA classification
FDA Class 2 ·System, Cystic Fibrosis Transmembrane Conductance Regulator Gene, Variant Gene Sequence Detection

Upper Arm Electronic Blood Pressure Monitor (U87Y series (models including U80Y, U81Y, U82Y,U83Y,U86Y U80N, U81NH), U86E series (including U82E, U80E, U80EH, U81E, U83E, U85E, U80L, U87E ), U81X series (including U81X, U80X, U82X, U83X, U81D, U82D, U83D, U81RH, U82RH) and U83Z series (including U83Z, U80Z, U81Z, U82Z, U85Z, U86Z and U87Z))

FDA 510(k)
FDA Class 2 ·Cardiovascular

Flexor Tuohy-Borst Side-Arm Introducer, Ansel Modification; Flexor Check-Flo Introducer, Ansel Modification; Flexor Check-Flo Introducers, Ansel Modification with High-Flex Dilator and Hydrophilic Coating; Flexor Check-Flo Introducer Balkin Up and Over Contralateral Design; Flexor Up and Over Balkin Contralateral Introducer; Flexor Check-Flo Introducer, Raabe Modification; Flexor Check-Flo Performer Introducer

FDA 510(k)
FDA Class 2 ·Cardiovascular

System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection

FDA classification
FDA Class 2 ·System, Microarray-Based, Genome-Wide, Postnatal Chromosomal Abnormality Detection

Kit, Conception-Assist, Home Use

FDA classification
FDA Class 2 ·Kit, Conception-Assist, Home Use

Washer, Cleaner, Automated, Endoscope

FDA classification
FDA Class 2 ·Washer, Cleaner, Automated, Endoscope

Bed, Air Fluidized

FDA classification
FDA Class 2 ·Bed, Air Fluidized

Stimulator, Muscle, Powered, With Limited Output, For Muscle Conditioning

FDA classification
FDA Class 2 ·Stimulator, Muscle, Powered, With Limited Output, For Muscle Conditioning

Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain

FDA classification
FDA Class 2 ·Nonthermal Shortwave Therapy Device Indicated For Over The Counter Use For The Treatment Of Pain