Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
QSZ
2026-09-02
GEH
2026-09-02
Maverix Cryo Biopsy Pro (MCB Pro) (MCBP-1000); Maverix Cryo Cartridge (CC-1000)
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JWH
2026-09-01
SK Knee System
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JID
2026-09-01
AMI™ Plasma Cartridge, AMI™
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MHX
2026-09-01
Carescape ONE; Carescape Dock F0; TruSignal ECG MM; TruSignal PRES MM; TruSignal TEMP MM; TruSignal SpO2 MM 1.8M; TruSignal SpO2 MM 3.0M
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LNH
2026-09-01
MAGNETOM Free.Max; MAGNETOM Free.Star
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JDR
2026-09-01
Arthrex DynaNite Staples
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PGY
2026-09-01
RadiForce MX247W
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QSO
2026-09-01
PRIMED Chemotherapy Drug Tested Gowns (PM4-99450: PRIMED Chemotherapy Drug Tested Isolation Gown, Purple, AAMI Level 2; PM4-99460: PRIMED Chemotherapy Drug Tested Isolation Gown, Blue, AAMI Level 3)
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GCJ
2026-09-01
UNIDRIVE Select System
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HGX
2026-09-01
Wearable breast pump (Model: XN/MD-2249BS, ZFHF)
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GEX
2026-09-01
CO2 Laser System (MBT- CO2 Laser)
Ver detalhes →Nenhum dispositivo correspondente.
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