Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
QLQ
2026-08-14
LPN
2026-08-13
MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution
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NGX
2026-08-13
High Intensity Focused Electromagnetic Stimulation Device (FE60)
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LNH
2026-08-13
AIR Recon DL
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EBI
2026-08-13
UltraPrint Flexible Denture UV
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MSX
2026-08-13
Dashboard (P007000)
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KLW
2026-08-13
Levo Gen 2 Tinnitus Therapy System
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DXN
2026-08-13
Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)
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OLW
2026-08-13
BIS™ Advance pEEG Module
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GCJ
2026-08-13
VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)
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EMA
2026-08-13
Any-Cem
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DXN
2026-08-13
BP Go (BPP-855)
Ver detalles →No hay dispositivos coincidentes.
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