Beckman Coulter
Beckman Coulter holds FDA 510(k) medical device clearances, first cleared 2017, most recent 2024.
Top product codes for Beckman Coulter
Recent clearances by Beckman Coulter
- K232904 — Access Ostase
- K193124 — Unicel DxH 800 Coulter Cellular Analysis System
- K182886 — Cytomics FC 500 Series (MPL or MCL) Flow Cytometer
- K183592 — ClearLLab 10C Panels (B, T, M1, M2), Navios Flow Cytometer, Navios EX Flow Cytometer
- K181599 — Unicel DxH 800 Cellular Analysis System with Early Sepsis Indicator Application
- K181475 — DxH 520 Hematology Instrument
- DEN160047 — ClearLLab T1, ClearLLab T2, ClearLLab B1, ClearLLab B2, ClearLLab M
- K162897 — Navios EX Flow Cytometer, 6 Color/2 Laser, Navios EX Flow Cytometer, 8 Color/2 Laser, Navios EX Flow Cytometer, 10 Color/3 Laser
Data sourced from openFDA. This site is unofficial and independent of the FDA.