Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
OWN
2026-09-21
NBC
2026-09-21
Access NT-proBNP
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HIS
2026-09-21
FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male Latex Condoms – Aqueous Lubricant (Plain);FAMA Male Latex Condoms – Aqueous Lubricant (Ribbed);FAMA Male Latex Condoms – Aqueous Lubricant (Dotted);FAMA Male Latex Condoms – Aqueous Lubricant (Non-regular Shaped);MO Male Latex Condoms – Aqueous Lubricant (Ultra-thin);MO Male Latex Condoms – Aqueous Lubricant (Plain);MO Male Latex Condoms – Aqueous Lubricant (Ribbed);MO Male Latex Condoms – Aqueous Lubricant (Dotted);MO
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INI
2026-09-19
Electric Scooter (FDB08, FDB08A, FDB12)
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GEX
2026-09-19
Dynamis Pro Family
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GEX
2026-09-19
SmartIPL_NI System
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FED
2026-09-18
Pathfinder Endoscope Overtube
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CAF
2026-09-18
Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebulizer (UN209); Mesh Nebulizer (UN210)
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LGZ
2026-09-18
NORMOFLO™ Irrigation Fluid Warming Sets and Accessories (IR-601, IR-501, IR-61, PL-61)
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LLZ
2026-09-18
Elucid PlaqueIQ
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PTI
2026-09-18
25G Huber Needle
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HRS
2026-09-18
EnHAnce PEEK Bunion System
Ver detalhes →Nenhum dispositivo correspondente.
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