FDA applicant
Intl. Diagnostic Laboratories, Ltd.
FDA records 4 decisions for Intl. Diagnostic Laboratories, Ltd. (Israel, IL) from 1985 to 1987: 4 510(k) clearances. Most are in product codes MSJ (Apolipoproteins) and LIQ (Enzyme Linked Immunoabsorbent Assay, Rotavirus). 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 Laboratories, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Intl. Diagnostic Laboratories, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Intl. Diagnostic Laboratories, Ltd.’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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