FDA applicant

Ludlow Corp., Technical Papers Division

Chicopee, MA1 decision1990–19900 recalls

FDA records 1 decision for Ludlow Corp., Technical Papers Division (Chicopee, MA) in 1990: 1 510(k) clearance. All are in product code DRX (Electrode, Electrocardiograph). 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 Ludlow Corp., Technical Papers Division’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ludlow Corp., Technical Papers Division since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ludlow Corp., Technical Papers Division by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Ludlow Corp., Technical Papers Division’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Ludlow”

FDA records each applicant name separately; these may or may not be the same firm.

Ludlow Technical Products 5 The Ludlow Company LP 3

Ludlow Corp., Technical Papers Division

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ludlow”