FDA applicant

Paul Ritzau Pari GmbH

Germany, GR1 decision1992–19920 recalls

FDA records 1 decision for Paul Ritzau Pari GmbH (Germany, GR) in 1992: 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 GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paul Ritzau Pari GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Paul Ritzau Pari GmbH’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

Other applicant names beginning “Paul”

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

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

Paul Ritzau Pari GmbH

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Paul”