FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
JAQ
2024-10-29
ITI
2024-10-29
Electric Wheelchair (ME23-EW16-BC200-01); Electric Wheelchair (ME23-EW16-BC200-02)
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MBI
2024-10-29
OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor
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EOQ
2024-10-29
Video Bronchoscope System; Single-use Flexible Bronchoscope (BC-S1E00-L, BC-S1H00-L, BC-S1J00-L, BC-S1E00, BC-S1H00, BC-S1J00.); Digital Video Monitor (DVM-D1, DVM-D2)
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HWC
2024-10-29
Tigon Medical Fractures, Instability, and Reconstruction (FIRE)
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NWA
2024-10-29
TRACHEOBRONXANE™ DUMON®
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MBH
2024-10-29
Persona the Personalized Knee System
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OVD
2024-10-29
DeGen Medical Patient Specific Implant (PSI) System
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NRY
2024-10-29
Riptide Aspiration System
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CBP
2024-10-29
QualityFlow O2 Series (QualityFLOW O2); QualityFlow O2 Series (QualityFLOW O2 MTV)
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KNW
2024-10-29
Mammotome AutoCore™ Single Insertion Core Biopsy System
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GXH
2024-10-29
AtriCure cryoICE BOX (ACM)
View Details →No matching devices.
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