FDA applicant
Alcide Corp.
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
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.
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.
See the 510(k) Report