510(k) Report

FDA applicant

Pharmacia Hepar, Inc.

Franklin, OH1 decision1995–19950 recalls

FDA records 1 decision for Pharmacia Hepar, Inc. (Franklin, OH) in 1995: 1 510(k) clearance. All are in product code GGP (Test, Qualitative And Quantitative Factor…). 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, hematology panel, where it files most

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

FDA decisions per year

No FDA decision for Pharmacia Hepar, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pharmacia Hepar, 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 “Pharmacia”

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