Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
KPS
2016-01-12
FAD
2016-01-11
Universa Soft Ureteral Stents and Stent Sets
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JPA
2016-01-11
Sysmex Automated Blood Coagulation Analyzer CS-5100
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NUC
2016-01-11
K-Y Marilyn Pleasure Gel
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DZE
2016-01-11
PURE Ceramic Implants
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DYB
2016-01-11
Fortress Introducer Sheath SYstem
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DQY
2016-01-08
LONG SHEATH OR LS, 70 CM, LONG SHEATH OR LS, 80 CM, LONG SHEATH OR LS, 90 CM
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ERL
2016-01-08
Unidrive S III ENT 40701601-1 with KARL STORZ-SCB, DrillCut-X II Shaver Handpiece, High Speed EC Micromotor II for use with INTRA Drill Handpieces
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LEH
2016-01-08
ONLINE TDM Vancomycin Gen.3
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NBW
2016-01-08
MyGlucoHealth Wireless System
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EIH
2016-01-08
VINTAGE LD
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MQH
2016-01-08
Embryo Biopsy Pipette, Polar Body Biopsy Pipette, Testicular Sperm Extraction Pipette
Ver detalhes →Nenhum dispositivo correspondente.
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