Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
MBI
2026-09-02
EOQ
2026-09-02
3.8mm Slim ProVu Video Bronchoscope (090-02-0038U); 5.0mm Regular ProVu Video Bronchoscope (090-02-0050U); 6.0mm Large ProVu Video Bronchoscope (090-02-0060U); ProVu Video Bronchoscope 8 display (040-07-0082U)
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MBI
2026-09-02
Aevumed SUPERCYNCH™ Button System
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PHL
2026-09-02
Trexo Theo
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MUE
2026-09-02
I-View®
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LZO
2026-09-02
Momentum Acetabular Cup System
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GEX
2026-09-02
1927nm Thulium Laser System (PZ-DJG85-01, PZ-DJG85-02)
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GEI
2026-09-02
Ellian Enigma RF Device
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IYN
2026-09-02
Vivid Explorer/Vivid Advanced/Vivid Focus
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LZA
2026-09-02
Cardinal Health Nitrile Blue Examination Gloves Tested for Use with Chemotherapy Drugs and Fentanyl Citrate
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FOZ
2026-09-02
Ruby Intravascular Catheter
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LZG
2026-09-02
Pivot Insulin Delivery System
Ver detalhes →Nenhum dispositivo correspondente.
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