510(k) Report

FDA applicant

Devices and Diagnostics Consulting Group

Rockville, MD1 decision1998–19980 recalls

FDA records 1 decision for Devices and Diagnostics Consulting Group (Rockville, MD) in 1998: 1 510(k) clearance. All are in product code JMM (Column Chromatography & Color Development…). Its devices cite 1 predicate, 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 Devices and Diagnostics Consulting Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Devices and Diagnostics Consulting Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Devices and Diagnostics Consulting Group 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?

  • JMMColumn Chromatography & Color Development, Hydroxyproline1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K972788Crosslaps ElisaDevices and Diagnostics Consulting Group · 19981cites it

What has FDA decided for it lately?

  • K972788Crosslaps ElisaDevices and Diagnostics Consulting Group · 1998

The one decision as Devices and Diagnostics Consulting Group →