FDA 510(k) Clearances
510(k) cleared devices tracked by MedTracker
KPO
2025-04-04
LIT
2025-04-04
Passeo-35 Xeo Peripheral Dilatation Catheter; Passeo-18 Peripheral Dilatation Catheters; Passeo-14 Peripheral Dilatation Catheter; Oscar Peripheral Multifunctional Catheter System; Pantera Pro Percutaneous Transluminal Coronary Angioplasty Catheter; Pantera LEO Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter
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FRG
2025-04-04
Turbett Surgical Instrument Pod (TS1500); Turbett Surgical Instrument Pod (TS1200); Turbett Surgical Instrument Pod (TS1000)
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FMI
2025-04-04
K-Pack Enhance Needle (KH-2713RBBTC and KH-2913RBBTC)
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PTC
2025-04-04
UASure II Blood Uric Acid Monitoring System
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MAX
2025-04-04
Spectrum Spine Lumbar Cage System
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BTL
2025-04-04
VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)
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QEZ
2025-04-04
JETi Hydrodynamic Thrombectomy System
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QHA
2025-04-04
QFR (3.0)
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QIH
2025-04-03
syngo Dynamics (Version VA41D)
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IYN
2025-04-03
Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System
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DPS
2025-04-03
Masimo W1
View Details →No matching devices.
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