510(k) Report

FDA applicant

K & S Medicorp

Miami, FL3 decisions1986–19860 recalls

FDA records 3 decisions for K & S Medicorp (Miami, FL) in 1986: 3 510(k) clearances. Most are in product codes LDE (Stethoscope, Manual) and DQD (Stethoscope, Electronic). 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 K & S Medicorp’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for K & S Medicorp since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — K & S Medicorp 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?

  • LDEStethoscope, Manual1decision
  • DQDStethoscope, Electronic1decision
  • BZTStethoscope, Esophageal, With Electrical Conductors1decision

What has FDA decided for it lately?

  • K862131Saltzman Ear (TM) Endotracheal Ascultation ReceptorK & S Medicorp · 1986
  • K854772Transcor (TM) Radio-StethoscopeK & S Medicorp · 1986
  • K854771Saltzman Stethoscope HeadK & S Medicorp · 1986

All 3 as K & S Medicorp →