Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
KCT
2016-09-07
FRO
2016-09-07
Procellera
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CFR
2016-09-07
ELITech Clinical Systems GLUCOSE HK SL, ELITech Clinical Systems ELICAL 2, ELITech Clinical Systems ELITROL I and ELITROL II
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HGM
2016-09-07
Central Monitoring System
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FMI
2016-09-07
CareSens Pen Needle, Softip Pen Needle
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HRS
2016-09-07
Additive Orthopaedics Bone Wedge System
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GCJ
2016-09-07
Pelican Sling Retractor
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JWH
2016-09-07
GENflex2 Total Knee System
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HAE
2016-09-07
Symmetry Sharp Kerrison Rongeur
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FZP
2016-09-07
Weck Auto Endo10 Automatic Endoscopic Clip Applier
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FQH
2016-09-07
Next Science Irrigation Solution
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CGS
2016-09-07
ADVIA Chemistry Creatine Kinase (CK_L) Assay, ADVIA Chemistry Enzyme 3 Calibrator
Ver detalhes →Nenhum dispositivo correspondente.
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