510(k) Report

FDA applicant

D.L. Nelson and Assoc., Inc.

Atlanta, GA4 decisions1990–19950 recalls

FDA records 4 decisions for D.L. Nelson and Assoc., Inc. (Atlanta, GA) from 1990 to 1995: 4 510(k) clearances. Most are in product codes FWZ (Operating Room Accessories Table Tray) and HCY (Curette, Uterine). 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, general and plastic surgery panel, where it files most

How often FDA has decided D.L. Nelson and Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for D.L. Nelson and Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like D.L. Nelson and Assoc., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report