Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
FMZ
2026-07-28
IYN
2026-07-28
V8/XV8/XH8/H8/cV8/V8 ONE/XV8 ONE/XH8 ONE/H8 ONE/cV8 ONE Diagnostic Ultrasound System; V7/XV7/XH7/H7/cV7/V7 ONE/XV7 ONE/H7 ONE/XH7 ONE/cV7 ONE Diagnostic Ultrasound System; V6/XV6/XH6/H6/cV6/V6 ONE/XV6 ONE/H6 ONE/XH6 ONE/cV6 ONE Diagnostic Ultrasound System; V5/XV5/XH5/H5/cV5 Diagnostic Ultrasound System; V4/XV4/XH4/H4/cV4 Diagnostic Ultrasound System;
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KGO
2026-07-28
Latex Powder Free Surgical Gloves Tested for Use with Chemotherapy Drugs and Fentanyl Citrate; Latex Powder Free Surgical Gloves with Colloidal Oatmeal Tested for Use with Chemotherapy Drugs and Fentanyl Citrate
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KPS
2026-07-28
uMI Panvivo (uMI Panvivo M)
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QAX
2026-07-28
ELISIO™-HX
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QXM
2026-07-28
Revi System
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HRS
2026-07-28
Xpert Ankle
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QDQ
2026-07-28
See-Mode Augmented Reporting Tool, Breast (SMART-B)
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JAK
2026-07-28
BodyTom Elite (NL4000)
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QEZ
2026-07-27
Powered Aventus Thrombectomy System™
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PPN
2026-07-27
Shockwave Intravascular Lithotripsy (IVL) System with the Shockwave E8 Peripheral IVL Catheter
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LOX
2026-07-27
Euphora Rapid Exchange (RX) Balloon Dilatation Catheter
Ver detalhes →Nenhum dispositivo correspondente.
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