FDA applicant

Laboratoire Ccd C/O Washington Regulatory Services

Ringoes, NJ4 decisions1988–19890 recalls

FDA records 4 decisions for Laboratoire Ccd C/O Washington Regulatory Services (Ringoes, NJ) from 1988 to 1989: 4 510(k) clearances. Most are in product codes HHT (Spatula, Cervical, Cytological) and HFE (Brush, Endometrial). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Laboratoire Ccd C/O Washington Regulatory Services’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Laboratoire Ccd C/O Washington Regulatory Services since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Laboratoire Ccd C/O Washington Regulatory Services by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Laboratoire Ccd C/O Washington…’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 “Laboratoire”

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

Laboratoire Villanova 1 Laboratoire National D'Essais 1 Laboratoire Pan-Pra 1 Laboratoire Medix 1

Laboratoire Ccd C/O Washington Regulatory Services

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Laboratoire”