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510(k) K061794

FIDIS TM THYRO, MODEL MX002 by Biomedical Diagnostics (Bmd) SA — Product Code JZO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 21, 2006
Date Received
June 26, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Thyroid Autoantibody
Device Class
Class II
Regulation Number
866.5870
Review Panel
IM
Submission Type

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  • K070458 — MODIFICATION TO FIDIS VASCULITIS, MODEL MX007 (December 21, 2007)
  • K071210 — MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006 (December 19, 2007)
  • K060380 — FIDIS DSDNA (May 2, 2006)
  • K053383 — FIDIS CELIAC (March 29, 2006)
  • K053653 — FIDIS CONNECTIVE 10, MODEL MX006 (March 13, 2006)
  • K053012 — FIDIS VASCULITIS, MODEL MX007 (March 2, 2006)
  • K050286 — FIDIS CONNECTIVE 8 (October 3, 2005)

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  • K222610 — Elecsys Anti-Tg (September 15, 2023)
  • K193313 — Elecsys Anti-TSHR (February 27, 2020)
  • K151799 — EliA anti-TG Immunoassay, EliA anti-TPO Immunoassay, EliA Thyroid Positive Contr (March 25, 2016)
  • K152061 — IMMULITE 2000 TSI Assay, IMMULITE 2000 TSI Calibration Verification Material (March 3, 2016)
  • K092229 — THYRETAIN TM TSI REPORTER BIOASSAY (May 18, 2010)
  • K090760 — THERATEST EL-ANTI-TPO AND THERATEST EL-ANTI-THYROGLOBULIN, MODEL 104-119, 103-12 (September 3, 2009)
  • K083391 — THYROID STIMULATING IMMUNOGLOBULIN REPORTER ASSAY (May 21, 2009)