Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
NAY
2016-08-07
ITX
2016-08-05
Verza Guidance System
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LLZ
2016-08-05
QXLink
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NHA
2016-08-05
ArgenIS Titanium Abutments
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DQA
2016-08-05
Model 6100C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6100C Series: 6100CA, 6100CP, 6100CI, 6100CN), Model 6101C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6101C Series: 6101CA, 6101CP, 6101CI, 6101CN), Model 6102C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6102C Series: 6102CA, 6102CP, 6102CI, 6102CN), Model 8100AA/8100AP Reusable, Finger Clip Pulse Oximeter Sensor, Model 8101AA/8101AP Reusable, Finger Clip Pulse Oximeter Senso
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NHA
2016-08-05
Burn-out Cylinder and Angled Screw Abutments
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HEB
2016-08-05
Opal by Femtex Pull & Snap and Private Label Unscented Compact Applicator Tampon, RegularOpal by Femtex Pull & Snap and Private Label Unscented Compact Applicator Tampon, Super, Opal by Femtex Pull & Snap and Private Label Unscented Compact Applicator Tampon, Super Pl
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NBW
2016-08-05
On Call Pro Blood Glucose Monitoring System
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ELW
2016-08-05
Image Fast Set, Image Regular Set
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DQK
2016-08-05
EP-TRACER System
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PBZ
2016-08-05
Triton System
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IYN
2016-08-05
LOGIQ V5 Expert, LOGIQ V5, LOGIQ V3
Ver detalhes →Nenhum dispositivo correspondente.
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