FDA applicant

Precision Acoustics Ind., Inc.

New York, NY9 decisions1993–19940 recalls

FDA records 9 decisions for Precision Acoustics Ind., Inc. (New York, NY) from 1993 to 1994: 9 510(k) clearances. Most are in product codes EWO (Audiometer) and ETY (Tester, Auditory Impedance). 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, ear, nose and throat panel, where it files most

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

FDA decisions per year

No FDA decision for Precision Acoustics Ind., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Precision Acoustics Ind., Inc.

Which product codes does it file in?

What has FDA decided for it lately?