FDA applicant

Eg &G Wallac

Gaithersburg, MD1 decision1997–19970 recalls

FDA records 1 decision for Eg &G Wallac (Gaithersburg, MD) in 1997: 1 510(k) clearance. All are in product code JLW (Radioimmunoassay, Thyroid-Stimulating Hormone). 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, clinical chemistry panel, where it files most

How often FDA has decided Eg &G Wallac’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Eg &G Wallac since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Eg &G Wallac’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

Eg &G Wallac

Which product codes does it file in?

What has FDA decided for it lately?