FDA applicant

Compagnie DE Developpement Aguettant

Washington, DC1 decision1998–19980 recalls

FDA records 1 decision for Compagnie DE Developpement Aguettant (Washington, DC) in 1998: 1 510(k) clearance. All are in product code FRN (Pump, Infusion). 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, general hospital panel, where it files most

How often FDA has decided Compagnie DE Developpement Aguettant’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Compagnie DE Developpement Aguettant since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Compagnie DE Developpement Aguettant’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Compagnie”

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

Compagnie Oris Industrie, S.A. 2 Compagnie Financiere & Medicale (Cf&M) 1

Compagnie DE Developpement Aguettant

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Compagnie”