Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
OHT
2026-09-25
CAZ
2026-09-25
Profoject™ LOR Syringe
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QIH
2026-09-25
syngo.CT Brain Quantification
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JOJ
2026-09-25
3M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)
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BZD
2026-09-25
Altis Full Face Mask
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EMA
2026-09-25
EsTemp Implant
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NPM
2026-09-25
REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)
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QOF
2026-09-25
Xpert Respiratory Panel
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IYN
2026-09-25
EVO X30 Diagnostic Ultrasound System; EVO X20 Diagnostic Ultrasound System; EVO X10 Diagnostic Ultrasound System; EVO XP30 Diagnostic Ultrasound System; EVO XP20 Diagnostic Ultrasound System; EVO XP10 Diagnostic Ultrasound System; EVO XC30 Diagnostic Ultrasound System; EVO XC20 Diagnostic Ultrasound System; EVO XC10 Diagnostic Ultrasound System
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HWC
2026-09-25
Arthrex Beaming System
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HIH
2026-09-25
UNIDRIVE SIII System; HOPKINS Telescope 0º (26205AMA) Operating Sheath (26205CD) Obturator (26205OC) Shaver Blade (26205SA) Shaver Blade (26205SB) Shaver Blade (091133-01/-10) Shaver Blade (091134-01/-10)
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PEN
2026-09-24
QIAstat-Dx BCID GN Plus AMR Panel
Ver detalhes →Nenhum dispositivo correspondente.
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