Autorizaciones FDA 510(k)
Dispositivos autorizados mediante 510(k) seguidos por MedTracker
DXQ
2026-02-13
HGX
2026-02-13
Wearable Breast Pump (Model W12)
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KWQ
2026-02-12
Lumbar Spine Truss System - Plating Solution (LSTS-PS)
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FMK
2026-02-12
Heel Stick Safety Lancet (HHZ-II, HHZ-III, HHZ-IV)
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HRS
2026-02-12
Wrist Fracture System
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OWN
2026-02-12
IMAGE1 (TC400US); X-to-4U Adapter (TC040)
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CEM
2026-02-12
ISE indirect K for Gen.2; ISE indirect Na for Gen.2; ISE indirect Cl for Gen.2; cobas pro integrated solutions
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CFR
2026-02-12
Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions
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OWN
2026-02-12
L12 LED Light Source with AIM
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OHS
2026-02-12
LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)
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GCJ
2026-02-12
Saberscope™ Laparoscope (SAS-A-536L); Xenocor® Video Processing Unit (VPUX-1)
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KPI
2026-02-12
Well-Life Incontinence Stimulation System (WL-2405i(P))
Ver detalles →No hay dispositivos coincidentes.
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