FDA applicant
Via Medical Corp.
FDA records 4 decisions for Via Medical Corp. (San Diego, CA) from 1993 to 1996: 4 510(k) clearances. Most are in product codes LZF (Pump, Infusion, Analytical Sampling) and CCE (Analyzer, Gas, Oxygen, Partial Pressure…). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Via Medical Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Via Medical Corp. since 2007.
Recalls per year
1in 2013
2007high 1 (2013) · low 0 (2007)2026
Class I Class II/III not classified
Planning a device like Via Medical 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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