FDA applicant
Immuno Diagnostic Center, Inc.
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
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.
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.
See the 510(k) ReportOther applicant names beginning “Immuno”
FDA records each applicant name separately; these may or may not be the same firm.