Home / 510(k) Clearances / K050840

510(k) K050840

MODIFICATION TO DUET SYSTEM by Bioview , Ltd. — Product Code JOY

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 16, 2005
Date Received
April 1, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Automated Cell-Locating
Device Class
Class II
Regulation Number
864.5260
Review Panel
HE
Submission Type

Other clearances by Bioview , Ltd.

  • K130775 — DUET SYSTEM (May 9, 2014)
  • K061602 — DUET SYSTEM (January 23, 2007)
  • K040591 — DUET SYSTEM (September 16, 2004)
  • K030192 — DUET SYSTEM (August 20, 2003)

Other clearances for product code JOY

  • K243144 — X100/X100HT with Full Field Peripheral Blood Smear (PBS) Application (June 27, 2025)
  • K221309 — AI100 with Shonit (September 19, 2023)
  • K220013 — X100HT with Slide Loader with Full Field Peripheral Blood Smear (PBS) Applicatio (May 3, 2022)
  • K200595 — CellaVision DC-1, CellaVision DC-1 PPA (October 16, 2020)
  • K201301 — X100 with Full Field Peripheral Blood Smear (PBS) Application (October 2, 2020)
  • K182062 — Sysmex UD-10, Fully Automated Urine Particle Digital Imaging Device (October 30, 2018)
  • K171315 — Advanced RBC Application (August 1, 2017)
  • K102778 — CELLAVISION DM1200 WITH THE BODY FLUID APPLICTION (September 16, 2011)
  • K092116 — EASYCELL CELL LOCATOR (May 12, 2010)
  • K092868 — CELLAVISION DM1200 AUTOMATED HEMATOLOGY ANALYZER, MODEL XU-10127 (November 20, 2009)