FDA applicant

Perfusion Partners & Assoc., Inc.

Crofton, MD2 decisions2003–20070 recalls

FDA records 2 decisions for Perfusion Partners & Assoc., Inc. (Crofton, MD) from 2003 to 2007: 2 510(k) clearances. All are in product code JQC (Centrifuges (Micro, Ultra, Refrigerated) For…). 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, clinical chemistry panel, where it files most

How often FDA has decided Perfusion Partners & Assoc., 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 — Perfusion Partners & Assoc., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Perfusion Partners & Assoc., Inc.

Which product codes does it file in?

What has FDA decided for it lately?