FDA applicant

Endocrine-Metabolic Center

Mchenry, IL9 decisions1979–19820 recalls

FDA records 9 decisions for Endocrine-Metabolic Center (Mchenry, IL) from 1979 to 1982: 9 510(k) clearances. Most are in product codes DPB (Radioimmunoassay, Digoxin (125-I), Rabbit…) and CGJ (Radioimmunoassay, Follicle-Stimulating Hormone). 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, clinical chemistry panel, where it files most

How often FDA has decided Endocrine-Metabolic Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endocrine-Metabolic Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Endocrine-Metabolic Center’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 “Endocrine-Metabolic”

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

Endocrine Sciences Products 2 Endocrine Associates, Inc. 2

Endocrine-Metabolic Center

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Endocrine-Metabolic”