510(k) Report

FDA applicant

Paul Ritzau Pari-Werk GmbH

Richmond, VA1 decision1993–19930 recalls

FDA records 1 decision for Paul Ritzau Pari-Werk GmbH (Richmond, VA) in 1993: 1 510(k) clearance. All are in product code CAF (Nebulizer (Direct Patient Interface)). 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 Paul Ritzau Pari-Werk GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paul Ritzau Pari-Werk GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Paul Ritzau Pari-Werk GmbH 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?

  • CAFNebulizer (Direct Patient Interface)1decision

Who builds on its devices?

Later devices cite its devices 1 time; 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.

  • K926455Pari Filter/Valve SetPaul Ritzau Pari-Werk GmbH · 19931cites it

What has FDA decided for it lately?

  • K926455Pari Filter/Valve SetPaul Ritzau Pari-Werk GmbH · 1993

The one decision as Paul Ritzau Pari-Werk GmbH →

Other applicant names beginning “Paul”

FDA records each applicant name separately; these may or may not be the same firm.

Paul Hartmann Corp. 5Paul B. Elder Co. 3Paul B. Heller, D.M.D. 1Paul E. Jaffe, D.M.D. 1Paul H. Schneider Ent. 1Paul Weiser Co. 1Paul Ritzau Pari GmbH 1Paul S. Barclay, D.D.S., Ltd. 1