FDA applicant

Flowscan, Inc.

San Francisco, CA2 decisions1995–19950 recalls

FDA records 2 decisions for Flowscan, Inc. (San Francisco, CA) in 1995: 2 510(k) clearances. Most are in product codes DQD (Stethoscope, Electronic) and DQC (Phonocardiograph). 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 Flowscan, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Flowscan, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Flowscan, Inc.

Which product codes does it file in?

What has FDA decided for it lately?