FDA applicant

Algotek, Inc.

Palo Alto, CA2 decisions1985–19871 recall

FDA records 2 decisions for Algotek, Inc. (Palo Alto, CA) from 1985 to 1987: 2 510(k) clearances. Most are in product codes IKN (Electromyograph, Diagnostic) and GWJ (Stimulator, Auditory, Evoked Response). 1 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Algotek, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Algotek, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?