Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
HRS
2025-12-19
JEY
2025-12-19
Southern Craniomaxillofacial (CMF) System
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HGX
2025-12-19
Wearable Electric Breast Pump (YM-8803)
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CJE
2025-12-19
Tru Liver Health Test Panel
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FAD
2025-12-19
Endura™ Ureteral Stent and Stent Set
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IZL
2025-12-19
Airbile-100
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DRE
2025-12-19
ProtekDilate Vascular Access Kit
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LNH
2025-12-19
MAGNETOM Sola; MAGNETOM Altea; MAGNETOM Sola Fit; MAGNETOM Viato.Mobile; MAGNETOM Vida; MAGNETOM Lumina; MAGNETOM Vida Fit; MAGNETOM Flow.Elite; MAGNETOM Flow.Neo; MAGNETOM Flow.Rise
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KGN
2025-12-19
MatriDerm pluS+ Bi-Layer
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MXD
2025-12-18
Assert-IQ (DM5100)
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FDX
2025-12-18
Single Use Cytology Brush V (BC-V600P-3010)
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DQK
2025-12-18
HemoSphere Alta Advanced Monitoring Platform (ALTAALL1; ALTACR1; ALTASR1)
Ver detalles →No hay dispositivos coincidentes.
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