FDA applicant

Fisher Price

Washington, DC2 decisions1986–19940 recalls

FDA records 2 decisions for Fisher Price (Washington, DC) from 1986 to 1994: 2 510(k) clearances. Most are in product codes HQY (Sunglasses (Non-Prescription Including…) and KPN (Alarm, Conditioned Response Enuresis). 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, ophthalmic panel, where it files most

How often FDA has decided Fisher Price’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fisher Price since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fisher Price 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 & Paykel Allied Products, Ltd. 12 Fisher and Paykel Healthcare Limited 4 Fisher Imaging Corp. 3

Fisher Price

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fisher”