FDA applicant
Pharmacia Deltec, Inc.
FDA records 43 decisions for Pharmacia Deltec, Inc. (St. Paul, MN) from 1987 to 1995: 43 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and FPA (Set, Administration, Intravascular). 17 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Pharmacia Deltec, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pharmacia Deltec, Inc. since 2007.
Recalls per year
1in 2016
Class I Class II/III not classified
Planning a device like Pharmacia Deltec, Inc.’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 “Pharmacia”
FDA records each applicant name separately; these may or may not be the same firm.