510(k) Report

FDA applicant

Pall Corp.

East Hills, NY4 decisions1998–20210 recalls

FDA records 4 decisions for Pall Corp. (East Hills, NY) from 1998 to 2021: 4 510(k) clearances. Most are in product codes CAH (Filter, Bacterial, Breathing-Circuit) and CAC (Apparatus, Autotransfusion). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Pall Corporation”.

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 Pall Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021: 1
2007high 1 (2021) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pall Corp.’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 “Pall”

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