510(k) Report

FDA applicant

Cytomedix

Walker, MN1 decision2003–20030 recalls

FDA records 1 decision for Cytomedix (Walker, MN) in 2003: 1 510(k) clearance. All are in product code JQC (Centrifuges (Micro, Ultra, Refrigerated) For…). Its devices cite 2 predicates, 0 of them its own earlier devices. 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 Cytomedix’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cytomedix since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • JQCCentrifuges (Micro, Ultra, Refrigerated) For Clinical Use1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K030340Autologel Process Centrifuge, Model B4360 (100-103, 100-129)Cytomedix · 2003

The one decision as Cytomedix →