Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
GCJ
2016-02-12
JOH
2016-02-12
ProTrach Dualcare
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DQX
2016-02-12
Hornet Guidewire, Hornet 10 Guidewire, Hornet 14 Guidewire
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LLL
2016-02-12
QUANTA Flash Jo-1, QUANTA Flash Jo-1 Calibrators, and QUANTA Flash Jo-1 Ciontrols
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GAT
2016-02-12
HS SutureTape
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LZA
2016-02-12
Powder Free Nitrile Patient Examination Gloves, Blue Color
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GEX
2016-02-12
Tranberg CLS Laser Fiber
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FGE
2016-02-12
X-Suit NIR Biliary Metallic Stent
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LRC
2016-02-12
Relieva Scout Multi-Sinus Dilation System
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LLZ
2016-02-12
TraumaCad Mobile Release 2.0
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HWC
2016-02-12
MetaFix LS Locking Screws, Merete Cannulated PCS, Merete CS Cortical Screws, Merete Cannulated HCS, DuoThread Scarf Screws and TwistCut Snap-Off Screws
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DPS
2016-02-12
Digital Electrocardiograph
Ver detalhes →Nenhum dispositivo correspondente.
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