FDA applicant

Tyco Healthcare Nancy

Pleasanton, CA2 decisions2002–20030 recalls

FDA records 2 decisions for Tyco Healthcare Nancy (Pleasanton, CA) from 2002 to 2003: 2 510(k) clearances. All are in product code BZD (Ventilator, Non-Continuous (Respirator)). Its devices cite 3 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, anesthesiology panel, where it files most

How often FDA has decided Tyco Healthcare Nancy’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tyco Healthcare Nancy since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Tyco Healthcare Nancy’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 “Tyco”

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

Tyco Healthcare 14 Tyco Healthcare Group LP 6 Tyco Healthcare/Kendall 4 Tyco Intl. (Us), Inc. 1 Tyco Electronics Corporation 1 Tyco Healthcare Deutschaland GmbH 1

Tyco Healthcare Nancy

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Tyco”