Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
MYC
2026-09-11
HBC
2026-09-11
Surgical Power System
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BTO
2026-09-11
Venti-Trach Tracheostomy Tube (570 Series); Venti-Trach Tracheostomy Tube (571 Series); Venti-Trach Tracheostomy Tube (580 Series); Venti-Trach Tracheostomy Tube (581 Series)
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JOW
2026-09-11
Sequential Circulator (SC-4004-DL, SC-4008-DL)
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MLO
2026-09-11
ZBPro Diagnostic (Version 2.0)
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FRO
2026-09-11
SkinSmart Antimicrobial HydroGel
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QOF
2026-09-11
FINDER Flu A&B/SARS-CoV-2 Test
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QPC
2026-09-11
PRIMED AAMI Level 3 Open Back Gowns
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MQV
2026-09-11
Mg OSTEOREVIVE™;Mg OSTEOCRETE™
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KIF
2026-09-11
Vioseal X
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KGI
2026-09-11
BoneVue
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FET
2026-09-10
4K Camera Head OLYMPUS CH-S700-08-LB
Ver detalles →No hay dispositivos coincidentes.
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