FDA applicant

Ramco Laboratories, Inc.

Houston, TX9 decisions1981–19980 recalls

FDA records 9 decisions for Ramco Laboratories, Inc. (Houston, TX) from 1981 to 1998: 9 510(k) clearances. Most are in product codes GGP (Test, Qualitative And Quantitative Factor…) and GGT (Assay, Erythropoietin). Its devices cite 2 predicates, 1 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Ramco Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Ramco Laboratories, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?