Autorizações FDA 510(k)
Dispositivos autorizados via 510(k) acompanhados pelo MedTracker
LZO
2026-03-12
NRY
2026-03-12
Tigertriever 25 Revascularization Device
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HSB
2026-03-12
Affixus Retrograde Femoral Nailing System
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EHD
2026-03-12
Dental X-RAY Unit (AJX200)
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EZD
2026-03-12
Liv Pre-lubricated Intermittent Catheter
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HGX
2026-03-12
Mini Moon electric breast pump (PA221); Moon Wave electric breast pump (PA220)
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DTZ
2026-03-12
Quantum Perfusion Blood Oxygenator ECC VT160-E3 (VT160-E3); Quantum Perfusion Blood Oxygenator ECC VT200-E3 (VT200-E3); Quantum Perfusion Blood Oxygenator VT75- E3 (VT75- E3);
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IZL
2026-03-11
Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System
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OHT
2026-03-11
Hair Removal Device (CT10, CT10 Pro, CT11, CT11 Pro, CT12, CT12 Pro, CTU05, CTU07, CTU09, CTU012, CTU015, CTU X, DT015 Pro, DT015, DT017 Pro, DT017, DT025 Pro, DT025)
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EBF
2026-03-11
Venus Diamond; Venus Diamond Flow; Venus Pearl; Venus Bulk Flow One
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NAY
2026-03-11
da Vinci Force Feedback Instruments
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HRS
2026-03-11
Xpert Hand
Ver detalhes →Nenhum dispositivo correspondente.
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