Biokit USA, Inc.
Biokit USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1993.
Top product codes for Biokit USA, Inc.
Recent clearances by Biokit USA, Inc.
- K913467 — TOXOGEN
- K910541 — BIOKIT RPR
- K904310 — RHEUMAGEN RF T-CONTROL
- K910539 — RHEUMAJET RF
- K910686 — RHEUMAJET CRP
- K904311 — RHEUMAGEN ASO T-CONTROL
- K904312 — RHEUMAGEN CRP T-CONTROL
- K896433 — MODIFIED RUBAGEN
- K896271 — QUANTEX RF PLUS (LATEX, BUFFER STANDARD, CONTROL)
- K896272 — QUANTEX CRP PLUS (LATEX, BUFFER, STANDARD, CONTROL
- K894486 — QUANTEX ASO PLUS (LATEX,BUFFER STANDARD,CONTROL)
- K893755 — RUBAGEN
- K874678 — I.M.N. LATEX
- K854991 — REUMAGEN ASL
- K843741 — RPR TEST REDITEST
- K842256 — AS LATEX PLUS
Data sourced from openFDA. This site is unofficial and independent of the FDA.