510(k) Report

FDA applicant

Alcide Corp.

Redmond, WA4 decisions1985–19950 recalls

FDA records 4 decisions for Alcide Corp. (Redmond, WA) from 1985 to 1995: 4 510(k) clearances. Most are in product codes LRJ (Disinfectant, Medical Devices) and LIF (Dialyzer Reprocessing System). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Alcide Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Alcide Corp.’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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