Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
MBI
2016-08-03
FRO
2016-08-03
DURAFIBER Ag
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LLZ
2016-08-03
JointPoint
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KNW
2016-08-03
CASSI II Rotational Core Biopsy System
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BWF
2016-08-03
iPEP System and vPEP
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EMA
2016-08-03
IonoStar Plus
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DXT
2016-08-03
DyeVert NG Contrast Modulation System
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DZE
2016-08-03
IMMEDIATELOAD Dental Implant System
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HRS
2016-08-02
ARIX Foot System
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LZA
2016-08-02
Sterile Powder Free Nitrile Examination Gloves, Blue Colored. Tested For Use with Chemotherapy Drugs, with Non-Pyrogenic Labeling Claim
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KNW
2016-08-02
M-Biopsy Semi-Automatic Biopsy Instrument M-Biopsy Coaxial Introducer Needle for Sem
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HRS
2016-08-02
Biomet Microfixation Sternal Closure System
Ver detalhes →Nenhum dispositivo correspondente.
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