360 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FREEMAN/SAMUELSON TOTAL KNEE
FDA 510(k)
FDA Class 2
·Orthopedic
TRICON-M TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
RMC TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
KNEE, TOTAL, FEMORAL & TIBIAL
FDA 510(k)
FDA Class 2
·Orthopedic
TIBIAL PLATEU
FDA 510(k)
FDA Class 2
·Orthopedic
ICLH TIBIAL PLATEAU
FDA 510(k)
FDA Class 2
·Orthopedic
FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP
FDA 510(k)
FDA Class 2
·Orthopedic
MARK I TOTAL KNEE SYS. ARTHROPLASTY
FDA 510(k)
FDA Class 2
·Orthopedic
TRICON M TOTAL KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI APOLLO RELY SP OVER-THE-WIRE BALLOON DILATATION CATHETER WITH HYDRO/PEL COATING AND MINIQUET DEVICE
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI GRUNTZIG DILACA CORONARY ARTERY BALLOON DILATATION CATHETER & USCI XPRT WITH PRO/PEL COATING BALLOON DILATATION
Assay, Enzyme Linked Immunosorbent, Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·ORAQUICK HCV RAPID ANTIBODY TEST
DIGI-PRO TENS MODEL WL-2203 AND WL-2205
FDA 510(k)
FDA Class 2
·Neurology
TEMP SCAN
FDA 510(k)
FDA Class 2
·General Hospital
IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRAND
FDA 510(k)
FDA Class 2
·Neurology
THE IZZZY-TENS (WL-2401), THE SLIM-TENS (WL-2402), THE MENS-TENS (WL2403), THE COMPACT TENS (WL-2302)
FDA 510(k)
FDA Class 2
·Neurology
DIGI-PRO TENS, MODEL WL-2204 AND WL-2205
FDA 510(k)
FDA Class 2
·Physical Medicine
DIGI-PRO TENS/WL-2203B,2204B,2204B-P1,2204B-P2,2205B
FDA 510(k)
FDA Class 2
·Neurology
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R)PROCROSS(TM) OVER THE WIRE BALLON DILATATION CATHETERT WITH RELY TM BALLOON MATERIAL AND HYDRO/PEL