FDA applicant

Pharmacia Deutschland GmbH

Freiburg, DE10 decisions2002–20041 recall

FDA records 10 decisions for Pharmacia Deutschland GmbH (Freiburg, DE) from 2002 to 2004: 10 510(k) clearances. Most are in product codes MSV (System,Test,Antibodies,B2 - Glycoprotein I (B2…) and MID (System, Test, Anticardiolipin Immunological). 1 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, immunology panel, where it files most

How often FDA has decided Pharmacia Deutschland GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pharmacia Deutschland GmbH since 2007.

Recalls per year

1in 2012

2007high 1 (2012) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Pharmacia Deutschland GmbH’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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Other applicant names beginning “Pharmacia”

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

Pharmacia, Inc. 130 Pharmacia Deltec, Inc. 43 Pharmacia & Upjohn Co. 18 Pharmacia Diagnostics, Inc. 10 Pharmacia Eni Diagnostics, Inc. 2 Pharmacia Iovision, Inc. 1 Pharmacia Hepar, Inc. 1 Pharmacia Fine Chemicals 1

Pharmacia Deutschland GmbH

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Pharmacia”