FDA applicant

Fisher & Paykel Allied Products, Ltd.

Auckland, New Zealand, NZ12 decisions1982–19880 recalls

FDA records 12 decisions for Fisher & Paykel Allied Products, Ltd. (Auckland, New Zealand, NZ) from 1982 to 1988: 12 510(k) clearances. Most are in product codes BTT (Humidifier, Respiratory Gas, (Direct Patient…) and BXN (Stimulator, Nerve, Battery-Powered). 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 Fisher & Paykel Allied Products, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fisher & Paykel Allied Products, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fisher & Paykel Allied Products, 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 “Fisher”

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

Fisher Scientific Co., LLC 90 Fisher & Paykel Healthcare, Ltd. 83 Fisher & Paykel Electronics, Ltd. 17 Fisher Diagnostics 16 Fisher and Paykel Healthcare Limited 4 Fisher Imaging Corp. 3 Fisher Price 2

Fisher & Paykel Allied Products, Ltd.

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 “Fisher”