Biorent Diagnostic, Inc.
Biorent Diagnostic, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1983.
Top product codes for Biorent Diagnostic, Inc.
Recent clearances by Biorent Diagnostic, Inc.
- K832747 — ALBUMIN REAGENT SET
- K823060 — HEMOGLOBIN REAGENT
- K823211 — CK-UV REAGENT
- K822493 — OPTIMIZED UV-GOT REAGENT SET
- K822494 — OPTIMIZED UV-GPT REAGENT SET
- K822492 — OPTIMIZED UV-LDH REAGENT SET
- K820768 — COLORIMETRIC LDH REAGENT SET
- K820632 — COLORIMETRIC URIC ACID REAGENT SET
- K813555 — GLUCOSE ENZYME-COLOR REAGENT SET
- K813244 — UV URIC ACID DETERMINATION
- K811760 — CHOLESTEROL DETERMINATION
Data sourced from openFDA. This site is unofficial and independent of the FDA.