510(k) Report

FDA applicant

Nisha Communication Industries

Northbridge, CA2 decisions1998–20010 recalls

FDA records 2 decisions for Nisha Communication Industries (Northbridge, CA) from 1998 to 2001: 2 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and LIH (Interferential Current Therapy). 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 Nisha Communication Industries’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nisha Communication Industries since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nisha Communication Industries 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?

  • IPFStimulator, Muscle, Powered1decision
  • LIHInterferential Current Therapy1decision

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.

  • K980040Electronic Muscle Stimulator - Microstim J-1304DNisha Communication Industries · 19981cites it

What has FDA decided for it lately?

  • K993600Multi Interferential Stimulator, Model TR-841Nisha Communication Industries · 2001
  • K980040Electronic Muscle Stimulator - Microstim J-1304DNisha Communication Industries · 1998

All 2 as Nisha Communication Industries →