Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
FIE
2026-08-06
KRO
2026-08-06
Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee System
Ver detalhes →
PAM
2026-08-06
QIAstat-Dx BCID GPF Plus AMR Panel
Ver detalhes →
QNP
2026-08-05
CAD - Lower GI (EC07-01)
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MMK
2026-08-05
Huahong Sharps Container (HHR-I, HHR-II)
Ver detalhes →
KNY
2026-08-05
Transurethral Catheter Safety Valve (TUCSV) (80050)
Ver detalhes →
POW
2026-08-05
Ruthinium Disc
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N/D
2026-08-05
pVasc Net Mechanical Thrombectomy Device
Ver detalhes →
HAW
2026-08-05
Leksell® Vantage Stereotactic System
Ver detalhes →
OLR
2026-08-05
NaturaJel™ Oral Wound Care Kit
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EZD
2026-08-05
Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).
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EZL
2026-08-05
Rusch Latex Gold Foley Catheter
Ver detalhes →Nenhum dispositivo correspondente.
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