510(k) Report

FDA applicant

Immuno Diagnostic Center, Inc.

Dallas, TX3 decisions1990–19920 recalls

FDA records 3 decisions for Immuno Diagnostic Center, Inc. (Dallas, TX) from 1990 to 1992: 3 510(k) clearances. Most are in product codes DDR (Myoglobin, Antigen, Antiserum, Control) and JIR (Indicator Method, Protein Or Albumin (Urinary…). 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 Immuno Diagnostic Center, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Immuno Diagnostic Center, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Immuno Diagnostic Center, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Immuno”

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