510(k) Report

FDA applicant

Joseph A. Resnick

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Joseph A. Resnick (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code ILP (System, Communication, Non-Powered). 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, physical medicine panel, where it files most

How often FDA has decided Joseph A. Resnick’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Joseph A. Resnick since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Joseph A. Resnick’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

Which product codes does it file in?

  • ILPSystem, Communication, Non-Powered1decision

What has FDA decided for it lately?

  • K840112Speech TeacherJoseph A. Resnick · 1984

The one decision as Joseph A. Resnick →

Other applicant names beginning “Joseph”

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

Joseph M. Piocentile 1Joseph B. Marogil 1Joseph F. Daniel, C.R.N.A. 1Joseph A. Kott, M.D. 1