FDA applicant

Product Development Corp.

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Product Development Corp. (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code DWF (Catheter, Cannula And Tubing, Vascular…). 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 Product Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Product Development Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Product”

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

Product & Educational Services 4 Product and Educational Services, LLC 1 Product Research Organizations,Inc. 1 Product Development Industries, Inc. 1

Product Development Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Product”