Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
HKI
2026-01-16
DJG
2026-01-16
LZI Buprenorphine II Enzyme Immunoassay
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GKZ
2026-01-16
Tru Hematology Test
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BTT
2026-01-16
FL-10000U Respiratory Humidifier
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OWB
2026-01-16
Azurion R3.1
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ODP
2026-01-16
Curiteva Porous PEEK Cervical Interbody System; Curiteva Porous PEEK Lumbar Interbody System; Curiteva Porous PEEK Laminoplasty System; Curiteva Porous PEEK Standalone ALIF System
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PCH
2026-01-16
Xpert GI Panel
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DHB
2026-01-16
NOVEOS Specific IgE (sIgE): Capture Reagent F013, Peanut (Arachis hypogaea); Capture Reagent F076, Bos d 4 a-lactalbumin, Milk; Capture Reagent F077, Bos d 5 ß-lactoglobulin, Milk; Capture Reagent F232, Gal d 2 Ovalbumin, Egg
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NHB
2026-01-16
SeptAlign
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QJP
2026-01-16
Toro 88 Superbore Catheter
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NAY
2026-01-16
da Vinci Surgical System (IS5000)
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GZJ
2026-01-16
actiTENS mini
Ver detalles →No hay dispositivos coincidentes.
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