510(k) Report

FDA applicant

Via Medical Corp.

San Diego, CA4 decisions1993–19961 recall

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, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

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

2013: 1
2007high 1 (2013) · low 0 (2007)2026

Class I Class II/III not classified

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

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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