510(k) Report

FDA applicant

Fluidotherapy Corp.

Houston, TX3 decisions1983–19850 recalls

FDA records 3 decisions for Fluidotherapy Corp. (Houston, TX) from 1983 to 1985: 3 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and IMI (Ultrasonic Diathermy For Use In Applying…). 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 Fluidotherapy Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fluidotherapy Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fluidotherapy Corp. 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?

  • HCCDevice, Biofeedback1decision
  • IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat1decision
  • IMJDiathermy, Shortwave, For Use In Applying Therapeutic Deep Heat1decision

What has FDA decided for it lately?

  • K850573Curamed 402Fluidotherapy Corp. · 1985
  • K850640Sonopuls 434 Ultrasound Therapy EquipmentFluidotherapy Corp. · 1985
  • K832122Enraf NONIVS2 Channel Emg/Temp. FeedFluidotherapy Corp. · 1983

All 3 as Fluidotherapy Corp. →