FDA applicant

Gambro Services, Inc.

Minneapolis, MN1 decision2007–20070 recalls

FDA records 1 decision for Gambro Services, Inc. (Minneapolis, MN) in 2007: 1 510(k) clearance. All are in product code FIP (Subsystem, Water Purification). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Gambro Services, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Gambro Services, Inc.’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 “Gambro”

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

Gambro, Inc. 87 Gambro Renal Products 37 Gambro Healthcare 13 Gambro-Hospal, Inc. 3 Gambro Bct, Inc. 2 Gambro Renal Care Products 2 Gambro-Hosp-Cobe, Inc. 1

Gambro Services, Inc.

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?

Other applicant names beginning “Gambro”