510(k) Report

FDA applicant

Medical Accessories, Inc.

Trenton, NJ3 decisions1987–19920 recalls

FDA records 3 decisions for Medical Accessories, Inc. (Trenton, NJ) from 1987 to 1992: 3 510(k) clearances. Most are in product codes HGP (Electrode, Circular (Spiral), Scalp And…) and KNG (Monitor, Ultrasonic, Fetal). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Medical Accessories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Accessories, Inc. 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?

  • HGPElectrode, Circular (Spiral), Scalp And Applicator2decisions
  • KNGMonitor, Ultrasonic, Fetal1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K872057Fetal Scalp ElectrodeMedical Accessories, Inc. · 19871cites it

What has FDA decided for it lately?

  • K920056Pocket Size Fetal Heart DetectorMedical Accessories, Inc. · 1992
  • K901152Redyplate Disposable Leg PlateMedical Accessories, Inc. · 1990
  • K872057Fetal Scalp ElectrodeMedical Accessories, Inc. · 1987

All 3 as Medical Accessories, Inc. →