Intl. Diagnostic Technology
Intl. Diagnostic Technology holds FDA 510(k) medical device clearances, first cleared 1976, most recent 1985.
Top product codes for Intl. Diagnostic Technology
Recent clearances by Intl. Diagnostic Technology
- K850591 — FIAX TOXO-M ANTIBODIES TEST KIT
- K843570 — FIAX HAPTOGLOBIN TEST KIT
- K843621 — FIAX 420 DILUTOR
- K843356 — FIAX 100 FLUOROMETER
- K842749 — FIAX TOTAL IGE TEST KIT
- K842071 — FIAX TRANSFERRIN TEST KIT
- K841174 — RUBELLA ANTIBODY FLUOROIMMUNOASSAY
- K840867 — ALPHA-1-ANTITRYPSIN, FITC, ANTIGEN
- K834140 — ANTINUCLEAR ANTIBODY IMMUNOLOGICAL SYS
- K833984 — ANTINUCLEAR ANTIBODY IMMUNOLOGICAL
- K832821 — FIAX IGG TEST
- K832383 — IDT ANA STIQ ASSAY
- K832054 — FIAX CRP TEST KIT
- K831607 — FIAX IGA TEST KIT
- K831608 — FIAX IGM TEST KIT
- K831609 — FIAX IGG TEST KIT
- K830669 — FIAX COMPLEMENT C4 TEST KIT
- K830668 — FIAX COMPLEMENT C3 TEST KIT
- K812968 — FIAX RHEUMATOID FACTOR TEST KIT
- K801642 — FIAX TEST KIT FOR THEOPHYLLINE QUANT.
- K801308 — FIAX TEST KIT FOR TOBRAMYCIN QUANTITA
- K792559 — FIAX TEST KIT FOR HERPES SIMPLEX VIRUS
- K792249 — FIAX TEST KIT FOR ANTI-RUBELLA ANTIBOD
- K800032 — FIAX TEST KIT FOR GENTAMICIN QUAN.
- K791948 — FIAX TEST KIT FOR ANTI-CYTOMEGALORIRUS
- K790464 — FIAX TEST KIT FOR ANTI-TOXOPLASMA ANTIBO
- K761224 — ULTRA LOW LEVEL IMMUNOGLOBULIN G
- K761225 — LOW LEVEL HUMAN ALBUMIN TEST KITS
- K760206 — TEST, DETECTION, ANTINUCLEAR ANTIBODIES
Data sourced from openFDA. This site is unofficial and independent of the FDA.