FDA applicant
Intl. Diagnostic Technology
FDA records 29 decisions for Intl. Diagnostic Technology (Mchenry, IL) from 1976 to 1985: 29 510(k) clearances. Most are in product codes DHN (Antinuclear Antibody, Indirect…) and KTL (Anti-Dna Indirect Immunofluorescent Solid Phase). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Intl. Diagnostic Technology’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Intl. Diagnostic Technology since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Intl. Diagnostic Technology’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report