FDA applicant

Diagnostic Reagent Tech.

Mchenry, IL10 decisions1982–19840 recalls

FDA records 10 decisions for Diagnostic Reagent Tech. (Mchenry, IL) from 1982 to 1984: 10 510(k) clearances. Most are in product codes DGO (Ige, Peroxidase, Antigen, Antiserum, Control) and DHB (System, Test, Radioallergosorbent (Rast)…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, immunology panel, where it files most

How often FDA has decided Diagnostic Reagent Tech.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diagnostic Reagent Tech. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diagnostic Reagent Tech. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Diagnostic Reagent Tech.’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

Other applicant names beginning “Diagnostic”

FDA records each applicant name separately; these may or may not be the same firm.

Diagnostic Products Corp. 324 Diagnostic Systems Laboratories, Inc. 94 Diagnostic Chemicals, Ltd. (Usa) 77 Diagnostic Reagents, Inc. 66 Diagnostic Chemicals, Ltd. 66 Diagnostic Hybrids, Inc. 37 Diagnostic Technology, Inc. 28 Diagnostic Solutions, Inc. 26 Diagnostic Ultrasound Corp. 16 Diagnostic Systems 14 Diagnostic Specialties 8 Diagnostic Monitoring Software 5

Diagnostic Reagent Tech.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Diagnostic”