FDA applicant

Graseby Medical, Ltd.

Watford, Herts., GB5 decisions1992–19951 recall

FDA records 5 decisions for Graseby Medical, Ltd. (Watford, Herts., GB) from 1992 to 1995: 5 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and MEA (Pump, Infusion, Pca). 1 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, general hospital panel, where it files most

How often FDA has decided Graseby Medical, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Graseby Medical, Ltd. since 2007.

Recalls per year

1in 2017

2007high 1 (2017) · low 0 (2007)2026

Class I Class II/III not classified

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

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Other applicant names beginning “Graseby”

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

Graseby Andersen 1

Graseby Medical, Ltd.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Graseby”