Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
DRF
2016-11-15
PHX
2016-11-15
Aequalis PerFORM Reversed, Aequalis PerFORM+ Reversed Glenoid
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MRG
2016-11-15
IDS-iSYS 25VitDs, IDS-iSYS 25VitDs Control Set
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IZL
2016-11-15
Optima XR240amx
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KTT
2016-11-15
Hoffman LRF System
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IZL
2016-11-15
Digital Diagnostic Mobile X-ray System
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IYE
2016-11-15
CushionCast Moldable Cushions
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KDI
2016-11-15
Tablo Console
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FXX
2016-11-15
Protect U Guard Earloop and Tie-On Mask (Blue, White or Green)
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OAS
2016-11-15
X-MIND trium
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HQD
2016-11-15
SynergEyes A&M (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes KC (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes PS (paflufocon D hem-iberfilcon A) Hybrid Daily Wear Contact Lens, SynergEyes SiH (petrafocon A hem-larafilcon A) Hybrid Daily Wear Contact Lens, SynergEyes UltraHealth for Keratoconus (petrafocon A hem-larafilcon A) Hybrid Daily Wear Co
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FOZ
2016-11-15
AccuCath Intravascular Catheter
Ver detalhes →Nenhum dispositivo correspondente.
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