510(k) Report

FDA applicant

Hyland Therapeutic Div., Travenol Laboratories

Mchenry, IL44 decisions1976–19820 recalls

FDA records 44 decisions for Hyland Therapeutic Div., Travenol Laboratories (Mchenry, IL) from 1976 to 1982: 44 510(k) clearances. Most are in product codes JIX (Calibrator, Multi-Analyte Mixture) and LGO (Test, Leukocyte Typing). 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 Hyland Therapeutic Div., Travenol Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hyland Therapeutic Div., Travenol Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hyland Therapeutic Div., Travenol Laboratories by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hyland Therapeutic Div., Travenol…’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