510(k) Report

FDA applicant

Ppg Industries, Inc.

Pleasantville, NY20 decisions1987–19920 recalls

FDA records 20 decisions for Ppg Industries, Inc. (Pleasantville, NY) from 1987 to 1992: 20 510(k) clearances. Most are in product codes CHL (Electrode Measurement, Blood-Gases (Pco2, Po2)…) and DXO (Transducer, Pressure, Catheter Tip). 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 Ppg Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ppg Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ppg Industries, 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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