510(k) Report

FDA applicant

Stethoscope Technologies, Inc.

Mill Valley, CA1 decision2009–20090 recalls

FDA records 1 decision for Stethoscope Technologies, Inc. (Mill Valley, CA) in 2009: 1 510(k) clearance. All are in product code DQD (Stethoscope, Electronic). 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 Stethoscope Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009: 1
2009high 1 (2009) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Stethoscope Technologies, Inc. by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Stethoscope Technologies, 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?

  • DQDStethoscope, Electronic1decision

What has FDA decided for it lately?

  • K091972Milscope Floating Mass Stethoscope, Model 300-01Stethoscope Technologies, Inc. · 2009

The one decision as Stethoscope Technologies, Inc. →