Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
OLT
2026-08-19
MQG
2026-08-19
Wallace® Aspiration Pump (WAPV1); Wallace® Pump Filter Connector (WFC); Wallace® Vacuum Connection Kit (WVCK)
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KPO
2026-08-19
Nipro Dry Acid Concentrate Mixer
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HIF
2026-08-19
ENDOFLATOR+; Smart Smoke Evacuation
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ORZ
2026-08-18
TearCare System
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LZA
2026-08-18
NON-STERILE POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, WITH LICORICE ROOT EXTRACT AND UREA, TESTED FOR USE WITH CHEMOTHERAPY DRUGS, FENTANYL CITRATE, XYLAZINE HCl, AND GASTRIC ACID. OCEAN COLOR
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QSZ
2026-08-18
LUOFUCON® Wound Matrix
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QUW
2026-08-18
TeKBrace Solo Soft Tissue Reinforcement Device
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HIH
2026-08-18
HERizon RD5 Resecting Device (5FR1PK);HERizon RD5 Resecting Device - 5 pack (5FR5PK)
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QIH
2026-08-18
Lower Limb AI (LLAI)
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QJP
2026-08-18
p17 XR Microcatheter
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KHJ
2026-08-18
Tympendi™ (810)
Ver detalhes →Nenhum dispositivo correspondente.
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