FDA applicant

Nolan Biological Laboratories, Inc.

Mchenry, IL5 decisions1980–19810 recalls

FDA records 5 decisions for Nolan Biological Laboratories, Inc. (Mchenry, IL) from 1980 to 1981: 5 510(k) clearances. Most are in product codes JWW (Antigen, Cf, B. Dermatitidis) and GMI (Antigen, Cf And / Or Id, Coccidioides Immitis). 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, microbiology panel, where it files most

How often FDA has decided Nolan Biological Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nolan Biological Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nolan Biological Laboratories, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Nolan Biological Laboratories, 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) Report

Nolan Biological Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?