FDA applicant

Anco Medical Reagents & Assoc.

Mchenry, IL26 decisions1981–19840 recalls

FDA records 26 decisions for Anco Medical Reagents & Assoc. (Mchenry, IL) from 1981 to 1984: 26 510(k) clearances. Most are in product codes GHM (Test, Sickle Cell) and JIS (Calibrator, Primary). 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 Anco Medical Reagents & Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anco Medical Reagents & Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Anco Medical Reagents & Assoc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Anco Medical Reagents & Assoc.’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 “Anco”

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

Anco Merchandise Co., Ltd. 1

Anco Medical Reagents & Assoc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Anco”