FDA applicant

Polytechnic Resources, Inc.

Baltimore, MD1 decision2005–20050 recalls

FDA records 1 decision for Polytechnic Resources, Inc. (Baltimore, MD) in 2005: 1 510(k) clearance. All are in product code BZG (Spirometer, Diagnostic). 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, anesthesiology panel, where it files most

How often FDA has decided Polytechnic Resources, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Polytechnic Resources, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Polytechnic Resources, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Polytechnic Resources, Inc.

Which product codes does it file in?

What has FDA decided for it lately?