FDA applicant

Philadelphia Medical Specialties

Mchenry, IL6 decisions1981–19840 recalls

FDA records 6 decisions for Philadelphia Medical Specialties (Mchenry, IL) from 1981 to 1984: 6 510(k) clearances. Most are in product codes GWN (Nystagmograph) and GWM (Device, Monitoring, Intracranial Pressure). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Philadelphia Medical Specialties since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Philadelphia”

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

Philadelphia Biologics Center 11

Philadelphia Medical Specialties

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Philadelphia”