510(k) Report

FDA applicant

Lifestream Purfication Systems, LLC

Fort Worth, TX1 decision2002–20020 recalls

FDA records 1 decision for Lifestream Purfication Systems, LLC (Fort Worth, TX) in 2002: 1 510(k) clearance. All are in product code KPL (Colonic Irrigation System). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Lifestream Purfication Systems, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifestream Purfication Systems, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Lifestream Purfication Systems, LLC 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?

  • KPLColonic Irrigation System1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K003720Angel of Water Colon Hydrotherapy SystemLifestream Purfication Systems, LLC · 20022cite it

What has FDA decided for it lately?

  • K003720Angel of Water Colon Hydrotherapy SystemLifestream Purfication Systems, LLC · 2002

The one decision as Lifestream Purfication Systems, LLC →

Other applicant names beginning “Lifestream”

FDA records each applicant name separately; these may or may not be the same firm.

Lifestream Int'L, Inc. 23Lifestream Technologies, Inc. 3Lifestream Diagnostics, Inc. 1