FDA applicant

Nasiff Assoc., Inc.

Brewerton, NY5 decisions1990–20000 recalls

FDA records 5 decisions for Nasiff Assoc., Inc. (Brewerton, NY) from 1990 to 2000: 5 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and LOS (Unnamed device). 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 Nasiff Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nasiff Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Nasiff Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?