510(k) Report

FDA applicant

Netech Corporation

Farmingdale, NY2 decisions1996–20190 recalls

FDA records 2 decisions for Netech Corporation (Farmingdale, NY) from 1996 to 2019: 2 510(k) clearances. All are in product code DRL (Tester, Defibrillator). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Netech Corp.”.

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 Netech Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Netech Corporation’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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Which product codes does it file in?

  • DRLTester, Defibrillator2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K190437Delta 3300Netech Corporation · 2019
  • K961595Defibrillator Analyzer, Delta 1000Netech Corp. · 1996

The one decision as Netech Corporation →The one decision as Netech Corp. →