7,404 results
·
48ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
×
TRANSFLOW TEST
FDA 510(k)
FDA Class 2
·Anesthesiology
PARAPAC
FDA 510(k)
FDA Class 2
·Anesthesiology
BENCHMARK TRANSFER TEST
FDA 510(k)
FDA Class 2
·Anesthesiology
MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR
FDA 510(k)
FDA Class 2
·General Hospital
Lucid Q-PTP / HWA 55
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CRAFTMATIC ADJUSTABLE BEDS WITH OPTIONAL HEAT & MASSAGE, MODELS CRAFTMATIC MONACO, I, II, III & CLASSIC
FDA 510(k)
FDA Class 2
·General Hospital
uwe sun tanning beds/booths P90, iBED EVG, iSUN HP, SILVERBULLET SE, LOTUS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·OMNISENSE 7000S ULTRASOUND BONE SONOMETER
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·NEEDLE ZAP (R)
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·THE SUNLIGHT OMNISENSE(TM) ULTRASOUND BONE SONOMETER
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·OMNISENSE 7000S ULTRASOUND BONE SONOMETER
Sharps Needle Destruction Device
FDA Pre-Market Approval
FDA Class 2
·NEEDLE ZAP
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·SUNLIGHT OMNISENSE 7000S ULTRASOUND BONE SONOMETER
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·SUNLIGHT OMNISENSE 7000S
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·SUNLIGHT OMNISENSE ULTRASOUND BONE SONOMETER
Bone Sonometer
FDA Pre-Market Approval
FDA Class 2
·SUNLIGHT OMNISENSE BONE SONOMETER
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·LT-CAGE LUMBAR TAPERED FUSION DEVICE (TI AND PEEK)
Lithotriptor, Extracorporeal Shock-Wave, Urological
FDA Pre-Market Approval
FDA Class 2
·HMT SHOCK PLUG/LITHOTRIPTER ELECTRODE
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·HEPATITIS C CHECK TESTING SERVICE
Lenses, Soft Contact, Daily Wear
FDA Pre-Market Approval
FDA Class 2
·ADYPI (ETAFILCON A) HYDROPHILIC CONTACT LENS