FDA applicant

Hospal Medical Corp.

Mchenry, IL55 decisions1977–19890 recalls

FDA records 55 decisions for Hospal Medical Corp. (Mchenry, IL) from 1977 to 1989: 55 510(k) clearances. Most are in product codes KDI (Dialyzer, High Permeability With Or Without…) and FKQ (System, Dialysate Delivery, Central Multiple…). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Hospal Medical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hospal Medical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Hospal Medical Corp.’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 “Hospal”

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

Hospal Industrie 1 Hospal 1

Hospal Medical Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Hospal”