Reference Diagnostics, Inc.
Reference Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 2006.
Top product codes for Reference Diagnostics, Inc.
Recent clearances by Reference Diagnostics, Inc.
- K053211 — RDI HSFERRITIN KIT
- K053291 — FERRITIN CALIBRATOR SET, CATALOG NO. 8203
- K052148 — TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET
- K030044 — EXTENDED RANGE HS CRP KIT, CAT NO:9200
- K030772 — RDI EXTENDED RANGE CRP CALIBRATOR SET
- K021607 — RDI HS CRP CALIBRATOR SET
- K021609 — RDI HS CRP KIT
- K000783 — DIRECT TIBC CALIBRATOR
- K000781 — DIRECT TIBC KIT
- K990216 — MAGNETIC TIBC KIT
- K984107 — RDI DIRECT LDL CHOLESTEROL TEST
- K973988 — RDI HOMOGENEOUS HDL CHOLESTEROL TEST
- K964063 — RDI LDL PRECIPITATION REAGENT
- K964064 — RDI LIPIDIRECT MAGNETIC LDL REAGENT
- K944975 — MAGNETIC HDL CHOLESTEROL TEST
- K911906 — MAGNETIC HDL CHOLESTEROL TEST
- K893740 — LIPIDIRECT LOW DENSITY LIPOPROTEIN CHOLESTEROL TES
Data sourced from openFDA. This site is unofficial and independent of the FDA.