510(k) Report

FDA applicant

Technology Applications Assoc., Inc.

San Diego, CA1 decision1994–19940 recalls

FDA records 1 decision for Technology Applications Assoc., Inc. (San Diego, CA) in 1994: 1 510(k) clearance. All are in product code 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 Technology Applications Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Technology Applications Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Technology Applications Assoc., 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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