10,000 results
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149ms
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Sources: EU EUDAMED, US FDA
Filters
FDA FEI Number: 2011171
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Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·HEX WRENCH(MODEL 6501)
Z-BOX
FDA 510(k)
FDA Class 2
·Neurology
COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SCR WRAP
FDA 510(k)
FDA Class 2
·General Hospital
REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550, 04800, 05200, 06002, 02406, 04706, 04300,
FDA 510(k)
FDA Class 2
·Cardiovascular
DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
THE RINSPIRATOR, MODELS FG09770, FG08776, FG08777, FG08910
FDA 510(k)
FDA Class 2
·Cardiovascular
SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE
FDA 510(k)
FDA Class 2
·Cardiovascular
SILVERHAWK PERIPHERAL PLAQUE EXCISION SYSTEM, MODELS 02550,04800, 05200, 02406, 04706, 04300
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIOMETRICS DUALFLOW SWITCH BOX
FDA 510(k)
FDA Class 2
·Cardiovascular
NORFOLK/NORWICH PRESSURE INFUSION BOX
FDA 510(k)
FDA Class 1
·General Hospital
BASICS ENDOSCOPY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
COX DISPOSABLE RETRIEVAL DEVICES
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE EXCLUDER AAA ENDOPROSTHESIS
MOBICATH TRANSSEPTAL NEEDLE
FDA 510(k)
FDA Class 2
·Cardiovascular
Nexta PEEK Hammertoe Correction System
FDA 510(k)
FDA Class 2
·Orthopedic
PHOTEX DIODE LASER SERIES, MODELS 980, 810 AND 940
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BARD PTV DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Nextra CH Cannulated Hammertoe System
FDA 510(k)
FDA Class 2
·Orthopedic