FDA applicant

William Harvey Life Products Corp.

Mchenry, IL3 decisions1977–19810 recalls

FDA records 3 decisions for William Harvey Life Products Corp. (Mchenry, IL) from 1977 to 1981: 3 510(k) clearances. Most are in product codes HGX (Pump, Breast, Powered) and BYS (Oxygenator, Long Term Support Greater Than 6…). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided William Harvey Life Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for William Harvey Life Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like William Harvey Life Products Corp.’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

Other applicant names beginning “William”

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

William Cook Europe Aps 20 William A. Cook Australia Pty., Ltd. 14 William C. Nealon 1 William J. Forni, D.D.S. 1 William-Palmer Industries, Inc. 1 William E. Mckay 1 William Feinstein & Associates, Inc. 1 William Skidmore & Co., Ltd. 1 William K. Hagan 1 William F. Trinkaus 1 William Dixon Co. 1 William W. Wilkerson & Gregory A. Knutson 1

William Harvey Life Products Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “William”