510(k) Report

FDA applicant

Pryon Corp.

Menomonee Falls, WI4 decisions1992–19940 recalls

FDA records 4 decisions for Pryon Corp. (Menomonee Falls, WI) from 1992 to 1994: 4 510(k) clearances. Most are in product codes CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase) and DQA (Oximeter). 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 Pryon Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pryon Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase3decisions
  • DQAOximeter1decision

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K935272CAP 400 ATPryon Corp. · 19942cite it

What has FDA decided for it lately?

  • K942772A-200 Multi-Use Airway AdapterPryon Corp. · 1994
  • K935272CAP 400 ATPryon Corp. · 1994
  • K930250Low Dead Space Adaptor & Reuasable Airway AdaptorPryon Corp. · 1993
  • K915773P-300 Capnograph and Pulse OximeterPryon Corp. · 1992

All 4 as Pryon Corp. →