Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
GAW
2016-09-15
QSZ
2016-09-15
Mirragen Advanced Wound Matrix, 4x4”, Mirragen Advanced Wound Matrix, 2x2”, Mirragen Advanced Wound Matrix, 1x6”
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NUH
2016-09-15
HBOTC Muscle and Nerve Stimulator
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GEH
2016-09-15
Compound W Wart Removal System Dual Power
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CGA
2016-09-14
GEM Premier 3000
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PPS
2016-09-14
Flexitouch System
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NHA
2016-09-14
CAM Titanium Blanks
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OVE
2016-09-14
SeaSpine Shoreline ACS - Anterior Cervical Standalone System
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IYN
2016-09-14
EBit Series Diagnostic Ultrasound System
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HEX
2016-09-14
Colposcope System
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PPN
2016-09-14
Lithoplasty Peripheral Balloon Dilatation Catheter, Lithoplasty Generator and Connector Cable, Lithoplasty Connector Cable
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FRO
2016-09-14
ACTICOAT Surgical Dressing
Ver detalhes →Nenhum dispositivo correspondente.
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