FDA applicant
Pall Biomedical Products Co.
FDA records 28 decisions for Pall Biomedical Products Co. (Glen Cove, NY) from 1979 to 1997: 28 510(k) clearances. Most are in product codes FPB (Filter, Infusion Line) and DTM (Filter, Blood, Cardiopulmonary Bypass…). 4 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Pall Biomedical Products Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pall Biomedical Products Co. since 2007.
Recalls per year
1in 2025
Class I Class II/III not classified
Planning a device like Pall Biomedical Products Co.’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) ReportOther applicant names beginning “Pall”
FDA records each applicant name separately; these may or may not be the same firm.