FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
DRG
2025-10-02
FKX
2025-10-02
Archimedes Pro Automated Peritoneal Dialysis Cycler (3014-00000-1); Archimedes Standard Automated Peritoneal Dialysis Cycler (3014-00000-3); Archimedes Pro Disposable Tubing Set (3014-50000-1); Archimedes Standard Disposable Tubing Set (3014-50000-3); Archimedes Pro Plus Disposable Tubing Set (3014-50000-5)
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LLZ
2025-10-02
Philips IntelliSpace Cardiovascular
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DXN
2025-10-02
Upper Arm Electronic Blood Pressure Monitor (FC-BP107, FC-BP123, FC-BP125, FC-BP126, FC-BP127, FC-BP116)
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HWC
2025-10-02
Cannulated Screw and Kirschner (K wire) System
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JAK
2025-10-02
LungQ 4
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BYI
2025-10-02
BreatheBand® (Model 1000)
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LYK
2025-10-01
Vena MicroAngioscope™ System
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PBF
2025-10-01
Newclip Patient-matched instrumentation non sterile PSI
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QEP
2025-10-01
Visby Medical Men's Sexual Health Test
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GEI
2025-10-01
E Blator
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OHS
2025-10-01
Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)
View Details →No matching devices.
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