510(k) Report

FDA applicant

Precision Health Care Systems, Inc.

Torrance, CA1 decision1992–19920 recalls

FDA records 1 decision for Precision Health Care Systems, Inc. (Torrance, CA) in 1992: 1 510(k) clearance. All are in product code DQK (Computer, Diagnostic, Programmable). 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 Precision Health Care Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Precision Health Care Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Precision Health Care Systems, 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?

  • DQKComputer, Diagnostic, Programmable1decision

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.

  • K914577Rhythmscan Precision 6000Precision Health Care Systems, Inc. · 19922cite it

What has FDA decided for it lately?

  • K914577Rhythmscan Precision 6000Precision Health Care Systems, Inc. · 1992

The one decision as Precision Health Care Systems, Inc. →