510(k) Report

FDA applicant

G & W Applied Science Laboratories

Mchenry, IL4 decisions1978–19810 recalls

FDA records 4 decisions for G & W Applied Science Laboratories (Mchenry, IL) from 1978 to 1981: 4 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and DSF (Recorder, Paper Chart). 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 G & W Applied Science Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for G & W Applied Science Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — G & W Applied Science Laboratories by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive2decisions
  • DSFRecorder, Paper Chart1decision
  • ESDHearing Aid, Air-Conduction, Prescription1decision

What has FDA decided for it lately?

  • K813249Help-MateG & W Applied Science Laboratories · 1981
  • K780805S/D 600 Sphygmomanometer and PulsemeterG & W Applied Science Laboratories · 1978
  • K7806774600 RecorderG & W Applied Science Laboratories · 1978
  • K780566Health Seat SystemG & W Applied Science Laboratories · 1978

All 4 as G & W Applied Science Laboratories →