Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
PBX
2026-04-02
FOZ
2026-04-02
BD Insyte™ IV Catheter
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QBV
2026-04-02
SMART M-CELL PRP Concentration System
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LOX
2026-04-02
FLASH Flex™ Aorto-Ostial Angioplasty System
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QBV
2026-04-02
SMART M-CELL Bone Marrow Concentration System
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PHC
2026-04-02
LifeShield Infusion Safety Software Suite
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IRP
2026-04-02
Cryopush Cold Compression Device (A02-P-001)
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OWB
2026-04-02
BELLIGER ACE
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HSX
2026-04-02
Tahoe Unicondylar Knee System with TiNbN Overcoat
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SEP
2026-04-02
Onclarity™ Self-Collection Kit
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KPE
2026-04-02
Disposable Infusion Bag for Parenteral Nutrition
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JEY
2026-04-02
Leforte MMF System
Ver detalhes →Nenhum dispositivo correspondente.
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