510(k) Report

FDA applicant

Blue Ridge Media Co.

Mchenry, IL11 decisions1982–19820 recalls

FDA records 11 decisions for Blue Ridge Media Co. (Mchenry, IL) in 1982: 11 510(k) clearances. Most are in product codes JSE (Culture Media, Multiple Biochemical Test) and LHW (Erythrocyte Suspension, Multi Species…). 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 Blue Ridge Media Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Blue Ridge Media Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Blue Ridge Media Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Blue”

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