Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
SGT
2026-08-31
KPR
2026-08-31
MULTIX Impact; MULTIX Impact C
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OHS
2026-08-31
Facial Beauty Device (Facial Mask LED Beauty Device A-901; Facial LED & EMS Beauty Device A-902; Facial Mask LED & EMS Beauty Device A-907)
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FPB
2026-08-31
Lipipor NLF1A Infusion Filter, Lipipor NLF2A & NLF2NTA Infusion Filters, Lipipor TNA2A Infusion Filter
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OCC
2026-08-31
ID NOW Influenza A & B 2; ID NOW RSV; ID NOW Strep A 2; ID NOW COVID-19 2.0
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NFO
2026-08-31
SYNERJET PRO (SP-1003); InPhiuse (SP-1003); WOWJET (SP-1003)
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DXN
2026-08-31
Automatic Digital Blood Pressure monitor (LD-526)
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EBF
2026-08-31
Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)
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JOW
2026-08-31
Aerloom
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IYE
2026-08-31
EZFluence (RADEZ V2)
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HTY
2026-08-28
Primal K-Wire (P99-193-1410)
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PGX
2026-08-28
cobas Strep A Nucleic acid test for use on the cobas Liat System (07341911190); cobas Strep A Quality Control Kit (07402678190)
Ver detalhes →Nenhum dispositivo correspondente.
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