510(k) Report

FDA applicant

Stethographics, Inc.

Houston, TX2 decisions2002–20050 recalls

FDA records 2 decisions for Stethographics, Inc. (Houston, TX) from 2002 to 2005: 2 510(k) clearances. Most are in product codes BZM (Calculator, Pulmonary Function Interpretor…) and DQD (Stethoscope, Electronic). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Stethographics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Stethographics, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Stethographics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • BZMCalculator, Pulmonary Function Interpretor (Diagnostic)1decision
  • DQDStethoscope, Electronic1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K012387STG Multichannel Lung Sound Analysis SystemStethographics, Inc. · 20021cites it
  • K052283Heart STG System and SoftwareStethographics, Inc. · 20051cites it

What has FDA decided for it lately?

  • K052283Heart STG System and SoftwareStethographics, Inc. · 2005
  • K012387STG Multichannel Lung Sound Analysis SystemStethographics, Inc. · 2002

All 2 as Stethographics, Inc. →