510(k) Report

FDA applicant

Rjo Biologicals, Inc.

Kansas City, MO1 decision1987–19870 recalls

FDA records 1 decision for Rjo Biologicals, Inc. (Kansas City, MO) in 1987: 1 510(k) clearance. All are in product code KIS (Sera, Animal And Human). 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, hematology panel, where it files most

How often FDA has decided Rjo Biologicals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rjo Biologicals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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