FDA applicant

Anup Chakraborty Co.

Lincoln, NE1 decision1992–19920 recalls

FDA records 1 decision for Anup Chakraborty Co. (Lincoln, NE) in 1992: 1 510(k) clearance. All are in product code LDE (Stethoscope, Manual). 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 Anup Chakraborty Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anup Chakraborty Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Anup Chakraborty Co.

Which product codes does it file in?

What has FDA decided for it lately?