FDA applicant

Medrad/Technology For People

Mchenry, IL1 decision1983–19830 recalls

FDA records 1 decision for Medrad/Technology For People (Mchenry, IL) in 1983: 1 510(k) clearance. All are in product code DQO (Catheter, Intravascular, Diagnostic). 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 Medrad/Technology For People’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medrad/Technology For People since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medrad/Technology For People by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medrad/Technology For People’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 “Medrad/Technology”

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

Medrad, Inc. 105 Medrad Interventional/Possis 2 Medrad, Inc. / Bayer Medical Care, Inc. 2

Medrad/Technology For People

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medrad/Technology”