FDA applicant

Y. Daneshvar

Livonia, MI3 decisions1994–19960 recalls

FDA records 3 decisions for Y. Daneshvar (Livonia, MI) from 1994 to 1996: 3 510(k) clearances. All are in product code DXC (Clamp, Vascular). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Y. Daneshvar since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Y. Daneshvar

Which product codes does it file in?

What has FDA decided for it lately?